Retinitis Pigmentosa, Late-Adult Onset |
|
Rod-cone dystrophy |
OMIM:268025 |
Retinitis Pigmentosa, Y-Linked |
|
Rod-cone dystrophy |
OMIM:400004 |
Omphalocele, X-Linked |
|
Omphalocele |
OMIM:310980 |
Retinal Dysplasia, Primary |
|
Retinal dysplasia, Falciform retinal fold |
OMIM:312550 |
Retinitis Pigmentosa 55 |
|
Rod-cone dystrophy |
OMIM:613575 |
Cone-Rod Dystrophy, X-Linked, 2 |
|
Cone/cone-rod dystrophy, Cone dystrophy |
OMIM:300085 |
Omphalocele, Autosomal |
|
Omphalocele |
OMIM:164750 |
Retinitis Pigmentosa 67 |
|
Rod-cone dystrophy |
OMIM:615565 |
Retinitis Pigmentosa 24 |
|
Cone dystrophy, Rod-cone dystrophy |
OMIM:300155 |
Omphalocele |
|
Omphalocele |
ORPHA:660 |
Hernia, Double Inguinal |
|
Inguinal hernia |
OMIM:142350 |
Stargardt Disease 1 |
|
Macular degeneration, Retinitis pigmentosa inversa, Bull's eye maculopathy |
OMIM:248200 |
Retinal Dystrophy, Reticular Pigmentary, Of Posterior Pole |
|
Drusen, Reticular pigmentary degeneration, Retinal dystrophy |
OMIM:267800 |
Choroidal Dystrophy, Central Areolar, 3 |
|
Drusen, Chorioretinal atrophy |
OMIM:613144 |
Macular Degeneration, Age-Related, 11 |
|
Macular degeneration |
OMIM:611953 |
Atrophia Maculosa Varioliformis Cutis, Familial |
|
Macular atrophy |
OMIM:601341 |
Macular Degeneration, Age-Related, 4 |
|
Macular degeneration |
OMIM:610698 |
Macular Degeneration, Age-Related, 6 |
|
Macular degeneration |
OMIM:613757 |
Macular Degeneration, Age-Related, 7 |
|
Macular degeneration |
OMIM:610149 |
Macular Degeneration, Age-Related, 15 |
|
Macular degeneration |
OMIM:615591 |
Macular Degeneration, Age-Related, 2 |
|
Macular degeneration |
OMIM:153800 |
Choroidal Dystrophy, Central Areolar, 1 |
|
Pigmentary retinopathy, Chorioretinal atrophy, Choriocapillaris atrophy |
OMIM:215500 |
Gastroschisis |
|
Abdominal wall defect, Gastroschisis |
OMIM:230750 |
Macular Degeneration, Age-Related, 13 |
|
Drusen, Macular degeneration, Choroidal neovascularization, Macular scar |
OMIM:615439 |
Retinitis Pigmentosa 48 |
|
Macular degeneration, Rod-cone dystrophy |
OMIM:613827 |
Nuchal Bleb, Familial |
|
Stillbirth, Fetal cystic hygroma, Hydrops fetalis |
OMIM:257350 |
Indomethacin Embryofetopathy |
|
Multicystic kidney dysplasia, Renal insufficiency, Premature birth, Abnormal renal tubule morphol... |
ORPHA:1909 |
Night Blindness, Congenital Stationary, Type 1D |
|
Congenital stationary night blindness, Pigmentary retinopathy, Macular atrophy, Attenuation of re... |
OMIM:613830 |
Retinal Degeneration And Epilepsy |
|
Retinal degeneration |
OMIM:267740 |
Exudative Vitreoretinopathy 7 |
|
Retinal detachment, Exudative vitreoretinopathy, Retinal hole, Retinal fold, Retinal degeneration |
OMIM:617572 |
Retinitis Pigmentosa 36 |
|
Optic disc pallor, Bone spicule pigmentation of the retina, Macular degeneration, Rod-cone dystro... |
OMIM:610599 |
Renal Tubular Dysgenesis |
|
Anuria, Abnormality of the urinary system, Hypotension, Renotubular dysgenesis, Oligohydramnios |
OMIM:267430 |
Macular Degeneration, Early-Onset |
|
Macular degeneration, Choroidal neovascularization |
OMIM:616118 |
Stargardt Disease 4 |
|
Macular degeneration, Retinal flecks |
OMIM:603786 |
Exudative Vitreoretinopathy 3 |
|
Retinal detachment, Retinal exudate, Exudative vitreoretinopathy, Retinal hole, Retinal fold |
OMIM:605750 |
Macular Dystrophy, Retinal, 1, North Carolina Type |
|
Drusen, Macular dystrophy, Abnormality of macular pigmentation, Peripheral retinal atrophy |
OMIM:136550 |
Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 5 |
|
Anuria, Proteinuria, Hemolytic-uremic syndrome, Stage 5 chronic kidney disease, Hematuria, Hypert... |
OMIM:612925 |
Hydrops Fetalis, Nonimmune |
|
Congestive heart failure, Nonimmune hydrops fetalis, Hydrops fetalis |
OMIM:236750 |
Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 4 |
|
Anuria, Proteinuria, Hemolytic-uremic syndrome, Hematuria, Hypertension, Acute kidney injury |
OMIM:612924 |
Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 3 |
|
Anuria, Proteinuria, Hemolytic-uremic syndrome, Hematuria, Hypertension, Acute kidney injury |
OMIM:612923 |
Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 2 |
|
Anuria, Proteinuria, Hemolytic-uremic syndrome, Hematuria, Hypertension, Acute kidney injury |
OMIM:612922 |
Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 6 |
|
Anuria, Proteinuria, Hemolytic-uremic syndrome, Hematuria, Hypertension, Acute kidney injury |
OMIM:612926 |
Adenine Phosphoribosyltransferase Deficiency |
|
Renal insufficiency, Atrial fibrillation, Proteinuria, Dysuria, Recurrent urinary tract infection... |
ORPHA:976 |
Hemolytic Disease Of Fetus And Newborn, Rh-Induced |
|
Fetal ascites, Polyhydramnios, Hydrops fetalis, Fetal pericardial effusion, Fetal pleural effusion |
OMIM:619462 |
Macular Degeneration, Atrophic, X-Linked |
|
Macular degeneration |
OMIM:300834 |
Lymphatic Malformation 12 |
|
Inguinal hernia, Nonimmune hydrops fetalis, Fetal ascites, Polyhydramnios, Lymphedema, Fetal peri... |
OMIM:620014 |
Reese Retinal Dysplasia |
|
Remnants of the hyaloid vascular system, Retinal dysplasia |
OMIM:266400 |
Non-Syndromic Metopic Craniosynostosis |
|
Omphalocele |
ORPHA:3366 |
Retinoschisis 1, X-Linked, Juvenile |
|
Retinal detachment, Retinal atrophy, Retinal pigment epithelial atrophy, Mizuo phenomenon, Macula... |
OMIM:312700 |
X-Linked Retinal Dysplasia |
|
Abnormal retinal vascular morphology, Abnormality of retinal pigmentation, Retinal dysplasia |
ORPHA:1852 |
Fetal Encasement Syndrome |
|
Omphalocele, Decreased fetal movement, Congenital diaphragmatic hernia, Horseshoe kidney, Increas... |
OMIM:613630 |
Late-Onset Retinal Degeneration |
|
Sub-RPE deposits, Choroidal neovascularization, Chorioretinal degeneration, Retinopathy, Retinal ... |
OMIM:605670 |
Chromosome 1P36.33 Duplication Syndrome, Atad3 Gene Cluster, Autosomal Dominant |
|
Death in infancy, Hypospadias, Fetal akinesia sequence, Flexion contracture, Dilated cardiomyopat... |
OMIM:618815 |
Omphalocele-Cleft Palate Syndrome, Lethal |
|
Omphalocele |
OMIM:258320 |
Cardiomyopathy, Familial Restrictive, 6 |
|
Death in infancy, Pulmonary insufficiency, Tricuspid regurgitation, Hydrops fetalis, Pulmonic ste... |
OMIM:619433 |
Retinopathy, Pericentral Pigmentary, Dominant |
|
Bone spicule pigmentation of the retina, Retinal atrophy, Retinal dystrophy, Pigmentary retinopat... |
OMIM:180210 |
Achondrogenesis, Type Ib |
|
Inguinal hernia, Polyhydramnios, Edema, Breech presentation, Hydrops fetalis, Stillbirth, Umbilic... |
OMIM:600972 |
Long Qt Syndrome 3 |
|
Ventricular flutter, Nonimmune hydrops fetalis, Sudden cardiac death, Ventricular tachycardia, Hy... |
OMIM:603830 |
Idiopathic Neonatal Atrial Flutter |
|
Abnormal EKG, Abnormal atrioventricular conduction, Hydrops fetalis, Abnormal left ventricular fu... |
ORPHA:45452 |
Macular Degeneration, Age-Related, 1 |
|
Macular drusen, Choroidal neovascularization, Geographic atrophy, Macular hemorrhage, Macular deg... |
OMIM:603075 |
Polycystic Kidney Disease 7 |
|
Renal insufficiency, Renal atrophy, Stage 5 chronic kidney disease, Hypertension, Multiple renal ... |
OMIM:620056 |
Fetal Parvovirus Syndrome |
|
Hypertrophic cardiomyopathy, Increased nuchal translucency, Ascites, Hydrops fetalis |
ORPHA:295 |
Hydrops Fetalis |
|
Miscarriage, Nonimmune hydrops fetalis, Polyhydramnios, Lymphedema, Pericardial effusion, Abnorma... |
ORPHA:1041 |
Sorsby Pseudoinflammatory Fundus Dystrophy |
|
Retinal atrophy, Choroidal neovascularization, Retinal pigment epithelial atrophy, Macular dystro... |
ORPHA:59181 |
Polydactyly-Myopia Syndrome |
|
Inguinal hernia, Femoral hernia |
ORPHA:2917 |
Hemorrhagic Fever-Renal Syndrome |
|
Anuria, Acute tubulointerstitial nephritis, Intracranial hemorrhage, Tubulointerstitial nephritis... |
ORPHA:340 |
Miller-Dieker Syndrome |
|
Omphalocele, Nephropathy, Polyhydramnios |
ORPHA:531 |
Congenital Heart Block |
|
Premature birth, First degree atrioventricular block, Gallop rhythm, Pericardial effusion, Conges... |
ORPHA:60041 |
Pseudodiastrophic Dysplasia |
|
Omphalocele |
ORPHA:85174 |
Leber Congenital Amaurosis 19 |
|
Optic disc pallor, Retinal degeneration, Attenuation of retinal blood vessels |
OMIM:618513 |
Sialidosis Type 2 |
|
Inguinal hernia, Flexion contracture, Hydrops fetalis, Pedal edema, Umbilical hernia, Nephropathy... |
ORPHA:87876 |
Adenine Phosphoribosyltransferase Deficiency |
|
2,8-dihydroxyadenine crystalluria, Renal insufficiency, Urolithiasis, Nephrolithiasis, Oliguria, ... |
OMIM:614723 |
Hydrops Fetalis, Nonimmune, With Gracile Bones And Dysmorphism |
|
Hydrops fetalis, Nonimmune hydrops fetalis, Polyhydramnios |
OMIM:613124 |
Mitochondrial Complex I Deficiency, Nuclear Type 35 |
|
Elevated urinary 4-hydroxybutyric acid, Nonimmune hydrops fetalis, Lacticaciduria, Cardiomyopathy... |
OMIM:619003 |
Lymphatic Malformation 8 |
|
Nonimmune hydrops fetalis, Polyhydramnios, Pericardial effusion, Stillbirth, Pleural effusion, Ge... |
OMIM:618773 |
Familial Drusen |
|
Abnormality of retinal pigmentation, Macular drusen, Peripapillary chorioretinal atrophy, Choroid... |
ORPHA:75376 |
Glomerulopathy With Fibronectin Deposits 2 |
|
Renal insufficiency, Proteinuria, Glomerular deposits, Glomerulomegaly, Stage 5 chronic kidney di... |
OMIM:601894 |
Senior-Loken Syndrome 7 |
|
Retinal degeneration |
OMIM:613615 |
Focal Segmental Glomerulosclerosis 2 |
|
Proteinuria, Chronic kidney disease, Stage 5 chronic kidney disease, Focal segmental glomeruloscl... |
OMIM:603965 |
Developmental And Epileptic Encephalopathy 96 |
|
Death in infancy, Hydrops fetalis |
OMIM:619340 |
Coloboma Of Optic Nerve |
|
Retinal detachment, Optic disc coloboma |
OMIM:120430 |
Retinitis Pigmentosa 33 |
|
Optic disc pallor, Bone spicule pigmentation of the retina, Retinal pigment epithelial atrophy, R... |
OMIM:610359 |
Retinal Arterial Macroaneurysm With Supravalvular Pulmonic Stenosis |
|
Exudative retinal detachment, Retinal arterial macroaneurysms |
OMIM:614224 |
Duplication Of Urethra |
|
Urethral stricture, Recurrent urinary tract infections, Anuria, Hypospadias, Urinary incontinence... |
ORPHA:237 |
Fetal Valproate Spectrum Disorder |
|
Omphalocele |
ORPHA:1906 |
Systemic Capillary Leak Syndrome |
|
Renal insufficiency, Pericarditis, Abnormal renal tubule morphology, Myocarditis, Oliguria, Pedal... |
ORPHA:188 |
Coloboma Of Macula |
|
Macular coloboma |
OMIM:120300 |
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 2 |
|
Anuria, Megacystis, Pyelonephritis, Bidirectional shunt, Elevated pulmonary artery pressure, Feta... |
OMIM:619351 |
Renal Hypoplasia, Bilateral |
|
Premature birth, Proteinuria, Edema, Chronic kidney disease, Renal hypoplasia, Renal cyst, Oligur... |
ORPHA:97362 |
Glomerulopathy With Fibronectin Deposits 1 |
|
Glomerulopathy, Renal insufficiency, Proteinuria, Stage 5 chronic kidney disease, Lobular glomeru... |
OMIM:137950 |
Diffuse Neonatal Hemangiomatosis |
|
Renal insufficiency, Premature birth, Polyhydramnios, Renal hypoplasia/aplasia, Hydrops fetalis, ... |
ORPHA:2123 |
Glycogen Storage Disease Iv |
|
Decreased fetal movement, Polyhydramnios, Edema, Portal hypertension, Hydrops fetalis, Cardiomyop... |
OMIM:232500 |
Congenital Disorder Of Glycosylation, Type Ik |
|
Death in infancy, Nonimmune hydrops fetalis, Flexion contracture, Cardiomyopathy, Abnormality of ... |
OMIM:608540 |
Persistent Mullerian Duct Syndrome, Types I And Ii |
|
Inguinal hernia |
OMIM:261550 |
Chorioretinal Atrophy, Progressive Bifocal |
|
Retinal detachment, Chorioretinal dystrophy, Chorioretinal atrophy |
OMIM:600790 |
Retinitis Pigmentosa 70 |
|
Optic disc pallor, Macular degeneration, Rod-cone dystrophy, Retinal degeneration, Attenuation of... |
OMIM:615922 |
Infantile Sialic Acid Storage Disease |
|
Premature birth, Congestive heart failure, Hydrops fetalis, Nephrotic syndrome, Death in childhoo... |
OMIM:269920 |
Birdshot Chorioretinopathy |
|
Retinal detachment, Optic disc pallor, Abnormal chorioretinal morphology, Choroidal neovasculariz... |
ORPHA:179 |
Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1 |
|
Hemolytic-uremic syndrome, Hypertension, Anuria, Acute kidney injury |
OMIM:235400 |
Retinitis Pigmentosa 50 |
|
Retinal detachment, Optic disc pallor, Retinal flecks, Rod-cone dystrophy, Attenuation of retinal... |
OMIM:613194 |
Hypouricemia, Renal, 1 |
|
Proteinuria, Urolithiasis, Oliguria, Renal tubular epithelial necrosis, Hyperuricosuria, Renal co... |
OMIM:220150 |
Focal Segmental Glomerulosclerosis 5 |
|
Proteinuria, Stage 5 chronic kidney disease, Focal segmental glomerulosclerosis, Hypertension, Mi... |
OMIM:613237 |
Fetal Gaucher Disease |
|
Decreased fetal movement, Death in infancy, Fetal akinesia sequence, Flexion contracture, Hydrops... |
ORPHA:85212 |
Focal Segmental Glomerulosclerosis 3, Susceptibility To |
|
Renal insufficiency, Proteinuria, Hematuria, Focal segmental glomerulosclerosis, Hypertension |
OMIM:607832 |
Rhiny |
|
Inguinal hernia |
OMIM:180360 |
Retinitis Pigmentosa 32 |
|
Optic disc pallor, Bone spicule pigmentation of the retina, Pigmentary retinopathy, Photoreceptor... |
OMIM:609913 |
Cardiogenic Shock |
|
Abnormal EKG, Increased pulmonary capillary wedge pressure, Cardiac arrest, Myocardial infarction... |
ORPHA:97292 |
Achondrogenesis |
|
Thickened nuchal skin fold, Inguinal hernia, Polyhydramnios, Hydrops fetalis, Umbilical hernia |
ORPHA:932 |
Chondrodysplasia, Blomstrand Type |
|
Premature birth, Fetal ascites, Polyhydramnios, Hydrops fetalis, Stillbirth |
OMIM:215045 |
Neuraminidase Deficiency |
|
Inguinal hernia, Urinary excretion of sialylated oligosaccharides, Proteinuria, Facial edema, Inc... |
OMIM:256550 |
Congenital Pulmonary Lymphangiectasia |
|
Tricuspid regurgitation, Congestive heart failure, Hydrops fetalis, Chylopericardium, Pulmonic st... |
ORPHA:2414 |
Boomerang Dysplasia |
|
Omphalocele, Aplasia/Hypoplasia of the abdominal wall musculature, Hydrops fetalis, Polyhydramnios |
ORPHA:1263 |
Hypothyroidism, Congenital, Nongoitrous, 4 |
|
Omphalocele, Umbilical hernia |
OMIM:275100 |
Iga Nephropathy, Susceptibility To, 2 |
|
Proteinuria, Stage 5 chronic kidney disease, Hematuria, Hypertension, Nephritis, IgA deposition i... |
OMIM:613944 |
Infection-Related Hemolytic Uremic Syndrome |
|
Anuria, Edema, Myocarditis, Oliguria, Hypertension, Pleural empyema, Acute kidney injury, Nephrot... |
ORPHA:544482 |
Iga Nephropathy, Susceptibility To, 3 |
|
Proteinuria, Mesangial hypercellularity, Stage 5 chronic kidney disease, Hematuria, Hypertension,... |
OMIM:616818 |
Dysplastic Cortical Hyperostosis, Kozlowski-Tsuruta Type |
|
Abnormality of the urinary system, Hydrops fetalis, Polyhydramnios |
ORPHA:2204 |
Retinitis Pigmentosa 13 |
|
Bone spicule pigmentation of the retina, Optic disc drusen, Perifoveal ring of hyperautofluoresce... |
OMIM:600059 |
Lymphatic Malformation 1 |
|
Urethral stricture, Predominantly lower limb lymphedema, Nonimmune hydrops fetalis, Hyperkeratosi... |
OMIM:153100 |
Fibronectin Glomerulopathy |
|
Glomerulopathy, Renal insufficiency, Proteinuria, Cerebral hemorrhage, Pedal edema, Nephrotic syn... |
ORPHA:84090 |
Nail-Patella-Like Renal Disease |
|
Glomerulopathy, Renal insufficiency, Proteinuria, Hypertension, Microscopic hematuria |
ORPHA:2613 |
Myopia 3, Autosomal Dominant |
|
Retinal detachment |
OMIM:603221 |
Myopia 25, Autosomal Dominant |
|
Retinal detachment |
OMIM:617238 |
Myopia 2, Autosomal Dominant |
|
Retinal detachment |
OMIM:160700 |
Myopia 5, Autosomal Dominant |
|
Retinal detachment |
OMIM:608474 |
Primary Membranoproliferative Glomerulonephritis |
|
Renal insufficiency, Proteinuria, Myocardial infarction, Chronic kidney disease, Stage 5 chronic ... |
ORPHA:54370 |
Renal Failure, Progressive, With Hypertension |
|
Renal insufficiency, Proteinuria, Stage 5 chronic kidney disease, Hypertension, Microscopic hemat... |
OMIM:161900 |
Cervical Ribs, Sprengel Anomaly, Anal Atresia, And Urethral Obstruction |
|
Omphalocele, Renal hypoplasia, Hypertrophy of the urinary bladder, Urethral obstruction, Prune be... |
OMIM:601389 |
Isolated Anencephaly |
|
Omphalocele, Congenital diaphragmatic hernia |
ORPHA:563609 |
Klippel-Trénaunay Syndrome |
|
Gastrointestinal hemorrhage, Edema, Pulmonary embolism, Congestive heart failure, Hydrops fetalis... |
ORPHA:90308 |
Bladder Exstrophy |
|
Omphalocele, Hypoplasia of penis, Inguinal hernia, Recurrent urinary tract infections, Epispadias... |
ORPHA:93930 |
Achondrogenesis Type 1B |
|
Thickened nuchal skin fold, Femoral hernia, Polyhydramnios, Hydrops fetalis, Umbilical hernia |
ORPHA:93298 |
Focal Segmental Glomerulosclerosis 1 |
|
Proteinuria, Edema, Stage 5 chronic kidney disease, Focal segmental glomerulosclerosis, Hypertens... |
OMIM:603278 |
Free Sialic Acid Storage Disease |
|
Proteinuria, Aplasia/Hypoplasia of the abdominal wall musculature, Hydrops fetalis, Nephrotic syn... |
ORPHA:834 |
Diaphragmatic Defect-Limb Deficiency-Skull Defect Syndrome |
|
Omphalocele, Congenital diaphragmatic hernia |
ORPHA:2141 |
Irvan Syndrome |
|
Retinal detachment, Vitreous floaters, Optic atrophy, Macular edema, Retinal exudate, Tractional ... |
ORPHA:209943 |
Shiga Toxin-Associated Hemolytic Uremic Syndrome |
|
Anuria, Myocardial infarction, Dehydration, Hemoglobinuria, Hypertension, Acute kidney injury |
ORPHA:90038 |
Retinal Dystrophy And Obesity |
|
Retinal detachment, Retinal pigment epithelial atrophy, Retinal dystrophy, Retinal dots, Peripapi... |
OMIM:616188 |
Hb Bart'S Hydrops Fetalis |
|
Pericarditis, Polyhydramnios, Congestive heart failure, Hydrops fetalis, Oligohydramnios |
ORPHA:163596 |
Vitreoretinal Degeneration, Snowflake Type |
|
Retinal detachment, Snowflake vitreoretinal degeneration, Optically empty vitreous, Retinal dots |
OMIM:193230 |
Achondrogenesis Type 1A |
|
Thickened nuchal skin fold, Femoral hernia, Polyhydramnios, Hydrops fetalis, Umbilical hernia |
ORPHA:93299 |
Diffuse Cutaneous Systemic Sclerosis |
|
Renal insufficiency, Telangiectasia of the skin, Congestive heart failure, Flexion contracture, X... |
ORPHA:220393 |
Cardiomyopathy, Familial Hypertrophic, 27 |
|
Prolonged QT interval, Tricuspid regurgitation, Nonimmune hydrops fetalis, Cardiac arrest, Left v... |
OMIM:618052 |
Aneurysm Of Sinus Of Valsalva |
|
Aortic regurgitation, Edema, Congestive heart failure, Oliguria, Heart murmur |
ORPHA:1054 |
Lassa Fever |
|
Shock, Miscarriage, Premature birth, Facial edema, Oliguria |
ORPHA:99824 |
Car T Cell Therapy-Associated Cytokine Release Syndrome |
|
Tachycardia, Heart block, Capillary leak, Reduced left ventricular ejection fraction, Hypotension... |
ORPHA:542323 |
Lymphedema, Cardiac Septal Defects, And Characteristic Facies |
|
Omphalocele, Atrial flutter, Lymphedema, Hydrops fetalis, Oligohydramnios |
OMIM:601927 |
Acalvaria |
|
Omphalocele |
ORPHA:945 |
Transaldolase Deficiency |
|
Abnormality of the kidney, Hydrops fetalis, Edema, Telangiectasia |
ORPHA:101028 |
Fetal Akinesia, Respiratory Insufficiency, Microcephaly, Polymicrogyria, And Dysmorphic Facies |
|
Neonatal death, Inguinal hernia, Polyhydramnios, Fetal akinesia sequence |
OMIM:619602 |
Colonic Atresia |
|
Omphalocele, Gastroschisis |
ORPHA:1198 |
Gillessen-Kaesbach-Nishimura Syndrome |
|
Thickened nuchal skin fold, Omphalocele, Congenital diaphragmatic hernia, Polyhydramnios, Flexion... |
OMIM:263210 |
Bartter Syndrome, Type 4A, Neonatal, With Sensorineural Deafness |
|
Hyperchloriduria, Fetal polyuria, Global glomerulosclerosis, Premature birth, Renal insufficiency... |
OMIM:602522 |
Ulnar Agenesis And Endocardial Fibroelastosis |
|
Neonatal death, Hydrops fetalis |
OMIM:276822 |
Caudal Duplication |
|
Abnormal penis morphology, Ureteral duplication, Omphalocele, Renal hypoplasia/aplasia |
ORPHA:1756 |
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome |
|
Omphalocele, Death in infancy, Multicystic kidney dysplasia, Hydroureter, Polyhydramnios, Megacys... |
ORPHA:2241 |
Polycystic Kidney Disease 5 |
|
Stage 5 chronic kidney disease, Hypertension, Polycystic kidney dysplasia, Reduced renal corticom... |
OMIM:617610 |
Nephronophthisis 1 |
|
Polyuria, Tubular basement membrane disintegration, Stage 5 chronic kidney disease, Hypertension,... |
OMIM:256100 |
Idiopathic Steroid-Resistant Nephrotic Syndrome |
|
Diffuse mesangial sclerosis, Foamy urine, Proteinuria, Edema, Minimal change glomerulonephritis, ... |
ORPHA:567548 |
Exudative Vitreoretinopathy 2, X-Linked |
|
Retinal detachment, Peripheral retinal avascularization, Subretinal exudate, Intraretinal exudate... |
OMIM:305390 |
Trisomy 1Q |
|
Omphalocele, Multicystic kidney dysplasia, Camptodactyly of finger, Polyhydramnios, Congenital di... |
ORPHA:261344 |
Iga Nephropathy, Susceptibility To, 1 |
|
Proteinuria, Stage 5 chronic kidney disease, Hematuria, Hypertension, Nephritis, IgA deposition i... |
OMIM:161950 |
Schisis Association |
|
Omphalocele, Renal agenesis, Premature birth, Congenital diaphragmatic hernia |
ORPHA:63862 |
Trigonocephaly 1 |
|
Omphalocele, Long penis |
OMIM:190440 |
Hydrops, Lactic Acidosis, And Sideroblastic Anemia |
|
Nonimmune hydrops fetalis, Fetal pericardial effusion, Hematuria, Hypertension, Second degree atr... |
OMIM:617021 |
Diaphragmatic Defects, Limb Deficiencies, And Ossification Defects Of Skull |
|
Omphalocele, Congenital diaphragmatic hernia |
OMIM:601163 |
Lymphatic Malformation 7 |
|
Nonimmune hydrops fetalis, Edema, Lymphedema, Facial edema, Pericardial effusion, Increased nucha... |
OMIM:617300 |
Amyloidosis, Familial Visceral |
|
Proteinuria, Edema, Hematuria, Nephrotic syndrome, Hypertension, Nephropathy |
OMIM:105200 |
Donnai-Barrow Syndrome |
|
Omphalocele, Umbilical hernia, Proteinuria, Congenital diaphragmatic hernia |
ORPHA:2143 |
Cholera |
|
Tachycardia, Abnormality of renal excretion, Premature birth, Miscarriage, Dehydration, Hypovolem... |
ORPHA:173 |
Mulibrey Nanism |
|
Nephroblastoma, Congestive heart failure, Hydrops fetalis, Enamel hypoplasia, Ascites |
OMIM:253250 |
Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome |
|
Plantar telangiectasia, Predominantly lower limb lymphedema, Palpebral edema, Hydrops fetalis, Pa... |
ORPHA:69735 |
Kagami-Ogata Syndrome Due To Maternal 14Q32.2 Hypermethylation |
|
Omphalocele, Diastasis recti, Polyhydramnios, Large placenta, Umbilical hernia |
ORPHA:254534 |
Genetic Recurrent Myoglobinuria |
|
Dark urine, Renal insufficiency, Recurrent myoglobinuria, Exercise-induced myoglobinuria, Oliguri... |
ORPHA:99845 |
Osteochondrodysplasia, Complex Lethal, Symoens-Barnes-Gistelinck Type |
|
Hypospadias, Polyhydramnios, Flexion contracture, Hydrops fetalis, Micropenis, Hypertrophic cardi... |
OMIM:616897 |
Colchicine Poisoning |
|
Renal insufficiency, Congestive heart failure, Myocarditis, Hypovolemia, Oliguria, Dehydration, H... |
ORPHA:31824 |
Myopia, High, With Cataract And Vitreoretinal Degeneration |
|
Retinal detachment, Vitreous floaters, Peripheral vitreoretinal degeneration, Lattice retinal deg... |
OMIM:614292 |
Axial Mesodermal Dysplasia Spectrum |
|
Omphalocele, Premature birth, Congenital diaphragmatic hernia, Renal hypoplasia/aplasia, Abnormal... |
ORPHA:1834 |
Hypothyroidism, Congenital, Nongoitrous, 6 |
|
Omphalocele |
OMIM:614450 |
Microscopic Polyangiitis |
|
Gastrointestinal hemorrhage, Glomerulopathy, Renal insufficiency, Pericarditis, Epistaxis, Conges... |
ORPHA:727 |
Hypercalcemia, Infantile, 1 |
|
Polyuria, Nephrolithiasis, Dehydration, Hypercalciuria, Nephrocalcinosis, Medullary nephrocalcinosis |
OMIM:143880 |
Non-Syndromic Posterior Hypospadias |
|
Omphalocele, Congenital diaphragmatic hernia, Ventral shortening of foreskin, Urethral diverticul... |
ORPHA:95706 |
Epidermolysis Bullosa With Diaphragmatic Hernia |
|
Neonatal death, Congenital diaphragmatic hernia |
OMIM:226735 |
Congenital Myopathy 1B, Autosomal Recessive |
|
Decreased fetal movement, Hydrops fetalis, Polyhydramnios, Increased connective tissue |
OMIM:255320 |
Congenital Enterovirus Infection |
|
Decreased fetal movement, Premature birth, Fetal ascites, Polyhydramnios, Pericardial effusion, M... |
ORPHA:292 |
Exudative Vitreoretinopathy 1 |
|
Retinal detachment, Peripheral retinal avascularization, Vitreous floaters, Exudative vitreoretin... |
OMIM:133780 |
Ethylene Glycol Poisoning |
|
Prolonged QT interval, Shock, Renal insufficiency, Tachycardia, Atrial fibrillation, Congestive h... |
ORPHA:31826 |
Renal Hypoplasia |
|
Renal insufficiency, Urethral valve, Premature birth, Proteinuria, Unilateral renal agenesis, Rec... |
ORPHA:93101 |
Combined Oxidative Phosphorylation Deficiency 57 |
|
Death in infancy, Left ventricular noncompaction cardiomyopathy, Nonimmune hydrops fetalis, Cardi... |
OMIM:620167 |
Combined Oxidative Phosphorylation Deficiency 42 |
|
Death in infancy, Premature birth, Nonimmune hydrops fetalis, Cardiomyopathy, Neonatal death |
OMIM:618839 |
Combined Oxidative Phosphorylation Deficiency 40 |
|
Death in infancy, Premature birth, Nonimmune hydrops fetalis, Neonatal death, Hypertrophic cardio... |
OMIM:618835 |
Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome |
|
Reduced subcutaneous adipose tissue, Abnormal renal glomerulus morphology, Renal insufficiency, M... |
OMIM:137940 |
Gm1-Gangliosidosis, Type I |
|
Death in infancy, Inguinal hernia, Congestive heart failure, Dilated cardiomyopathy, Hydrops feta... |
OMIM:230500 |
Mucopolysaccharidosis Type 7 |
|
Inguinal hernia, Lymphedema, Hydrops fetalis, Mucopolysacchariduria, Umbilical hernia, Ascites |
ORPHA:584 |
Myopia 28, Autosomal Recessive |
|
Retinal detachment |
OMIM:619781 |
Carnitine-Acylcarnitine Translocase Deficiency |
|
Dicarboxylic aciduria, Ventricular tachycardia, Oliguria, Cardiomyopathy, Hypotension, Arrhythmia |
ORPHA:159 |
Vitreoretinopathy, Neovascular Inflammatory |
|
Peripheral retinal neovascularization, Retinal detachment, Large hyperpigmented retinal spots, Po... |
OMIM:193235 |
Nephronophthisis-Like Nephropathy 2 |
|
Renal insufficiency, Polyuria, Periglomerular fibrosis, Stage 5 chronic kidney disease, Tubular l... |
OMIM:619468 |
Lujo Hemorrhagic Fever |
|
Shock, Renal insufficiency, Facial edema, Periorbital edema, Myocarditis, Oliguria, Subconjunctiv... |
ORPHA:319213 |
Distal Duplication 15Q |
|
Omphalocele, Camptodactyly of finger |
ORPHA:1707 |
Hypercalcemia, Infantile, 2 |
|
Polyuria, Hypercalciuria, Renal phosphate wasting, Nephrocalcinosis, Medullary nephrocalcinosis |
OMIM:616963 |
Kagami-Ogata Syndrome Due To Maternal 14Q32.2 Microdeletion |
|
Omphalocele, Inguinal hernia, Diastasis recti, Polyhydramnios, Large placenta, Flexion contractur... |
ORPHA:254528 |
Yellow Fever |
|
Shock, Renal insufficiency, Anuria, Supraventricular arrhythmia, Hematemesis, Capillary leak, Red... |
ORPHA:99829 |
Campomelia, Cumming Type |
|
Death in infancy, Multicystic kidney dysplasia, Lymphedema, Hydrops fetalis, Multiple renal cysts... |
ORPHA:1318 |
Arthrogryposis, Cleft Palate, Craniosynostosis, And Impaired Intellectual Development |
|
Vesicoureteral reflux, Arthrogryposis multiplex congenita, Nonimmune hydrops fetalis, Hydronephrosis |
OMIM:618265 |
Umbilical Cord Ulceration-Intestinal Atresia Syndrome |
|
Single umbilical artery, Hydrops fetalis, Polyhydramnios |
ORPHA:3405 |
Senior-Loken Syndrome 4 |
|
Stage 5 chronic kidney disease, Polyuria, Nephronophthisis |
OMIM:606996 |
Vacterl/Vater Association |
|
Omphalocele, Hypoplasia of penis, Multicystic kidney dysplasia, Premature birth, Hypospadias, Pol... |
ORPHA:887 |
Persistent Müllerian Duct Syndrome |
|
Inguinal hernia |
ORPHA:2856 |
Cloverleaf Skull-Multiple Congenital Anomalies Syndrome |
|
Omphalocele |
ORPHA:93267 |
Sepsis In Premature Infants |
|
Tachycardia, Premature birth, Edema, Oliguria, Bradycardia, Reversible renal failure, Hypotension... |
ORPHA:90051 |
X-Linked Ehlers-Danlos Syndrome |
|
Umbilical hernia, Inguinal hernia, Hernia |
ORPHA:75497 |
Kagami-Ogata Syndrome |
|
Omphalocele, Inguinal hernia, Premature birth, Diastasis recti, Polyhydramnios, Flexion contractu... |
OMIM:608149 |
Combined Oxidative Phosphorylation Defect Type 27 |
|
Nonimmune hydrops fetalis |
ORPHA:477774 |
Hernia, Anterior Diaphragmatic |
|
Neonatal death, Congenital diaphragmatic hernia |
OMIM:306950 |
Fraser Syndrome 3 |
|
Sonographic non-visualized fetal bladder, Hypoplasia of the bladder, Hypoplasia of penis, Nonimmu... |
OMIM:617667 |
Mitochondrial Trifunctional Protein Deficiency 1 |
|
Congestive heart failure, Dilated cardiomyopathy, Hydrops fetalis, Abnormality of the amniotic fl... |
OMIM:609015 |
Trisomy 13 |
|
Abnormality of the ureter, Hydrops fetalis, Multiple renal cysts, Hernia, Displacement of the ure... |
ORPHA:3378 |
Arthrogryposis Multiplex Congenita 6 |
|
Decreased fetal movement, Death in infancy, Hypospadias, Polyhydramnios, Death in childhood, Neon... |
OMIM:619334 |
Cryoglobulinemia, Familial Mixed |
|
Proteinuria, Chronic kidney disease, Hematuria, Hypertension, Anasarca, Abnormal renal physiology |
OMIM:123550 |
Primary Hypomagnesemia With Hypercalciuria And Nephrocalcinosis With Severe Ocular Involvement |
|
Inguinal hernia, Nephrolithiasis, Hematuria, Umbilical hernia, Nephropathy |
ORPHA:2196 |
Lymphatic Malformation 6 |
|
Genital edema, Prune belly, Nonimmune hydrops fetalis, Polyhydramnios, Edema, Facial edema, Perio... |
OMIM:616843 |
Lymphangiectasia, Pulmonary, Congenital |
|
Palpebral edema, Nonimmune hydrops fetalis, Polyhydramnios, Edema, Facial edema, Chylous ascites,... |
OMIM:265300 |
Alg8-Cdg |
|
Premature birth, Abnormality of subcutaneous fat tissue, Edema, Hydrops fetalis, Camptodactyly, A... |
ORPHA:79325 |
Acute Monoblastic/Monocytic Leukemia |
|
Periorbital edema, Oliguria |
ORPHA:514 |
Cardiomyopathy, Dilated, 2G |
|
Aortic regurgitation, Tachycardia, Tricuspid regurgitation, Cerebral hemorrhage, Dilated cardiomy... |
OMIM:619897 |
Sucrosuria, Hiatus Hernia, And Impaired Intellectual Development |
|
Hiatus hernia |
OMIM:272000 |
Hypomagnesemia 7, Renal, With Or Without Dilated Cardiomyopathy |
|
Elevated left ventricular end-diastolic diameter, Polyuria, Dilated cardiomyopathy, Nephrocalcino... |
OMIM:620152 |
Cloacal Exstrophy |
|
Omphalocele, Hypoplasia of penis, Hydroureter, Ectopic kidney, Renal hypoplasia/aplasia, Horsesho... |
ORPHA:93929 |
Renal Glucosuria |
|
Glycosuria, Polyuria, Enuresis nocturna |
OMIM:233100 |
Brachial Amelia, Cleft Lip, And Holoprosencephaly |
|
Omphalocele |
OMIM:601357 |
Achondrogenesis, Type Ii |
|
Stillbirth, Polyhydramnios, Hydrops fetalis, Edema |
OMIM:200610 |
Tubulointerstitial Kidney Disease, Autosomal Dominant, 2 |
|
Renal cortical atrophy, Impaired renal uric acid clearance, Tubular basement membrane disintegrat... |
OMIM:174000 |
Nephronophthisis 3 |
|
Renal insufficiency, Polyuria, Stage 5 chronic kidney disease, Enuresis, Renal corticomedullary c... |
OMIM:604387 |
Posterior Urethral Valve |
|
Renal insufficiency, Recurrent urinary tract infections, Urinary incontinence, Dysuria, Fetal pye... |
ORPHA:93110 |
Mosaic Trisomy 1 |
|
Omphalocele, Camptodactyly of finger, Polyhydramnios, Congenital diaphragmatic hernia, Increased ... |
ORPHA:1692 |
Exstrophy-Epispadias Complex |
|
Urinary incontinence, Epispadias, Bladder duplication, Absent penis, Vesicoureteral reflux, Bladd... |
ORPHA:322 |
Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency |
|
Nonimmune hydrops fetalis, Polyhydramnios, Fetal akinesia sequence, Portal hypertension, Congesti... |
ORPHA:367 |
Denys-Drash Syndrome |
|
Proteinuria, Nephrotic syndrome, Hypertension, Nephropathy, Nephroblastoma |
ORPHA:220 |
Hemochromatosis, Neonatal |
|
Nonimmune hydrops fetalis, Oligohydramnios |
OMIM:231100 |
Gastrointestinal Defects And Immunodeficiency Syndrome 1 |
|
Omphalocele, Death in infancy, Polyhydramnios, Hematochezia, Congenital pulmonary airway malforma... |
OMIM:243150 |
Triploidy |
|
Omphalocele, Hypoplasia of penis, Hypospadias, Polyhydramnios |
ORPHA:3376 |
Bartter Syndrome, Type 5, Antenatal, Transient |
|
Fetal polyuria, Premature birth, Polyuria, Polyhydramnios, Hypercalciuria, Medullary nephrocalcin... |
OMIM:300971 |
Meckel Syndrome, Type 2 |
|
Omphalocele, Renal cyst |
OMIM:603194 |
Lymphatic Malformation 13 |
|
Nonimmune hydrops fetalis, Lymphedema, Fetal pericardial effusion, Single umbilical artery, Mitra... |
OMIM:620244 |
Congenital Disorder Of Glycosylation, Type Ia |
|
Death in infancy, Pericarditis, Proteinuria, Nonimmune hydrops fetalis, Edema, Pericardial effusi... |
OMIM:212065 |
Intellectual Developmental Disorder With Cardiac Defects And Dysmorphic Facies |
|
Omphalocele, Hypospadias |
OMIM:618316 |
Bartter Syndrome, Type 3 |
|
Hyperchloriduria, Impaired renal ltubular reabsorption of chloride, Polyuria, Renal salt wasting,... |
OMIM:607364 |
Gm1 Gangliosidosis |
|
Inguinal hernia, Premature birth, Camptodactyly of finger, Congestive heart failure, Aplasia/Hypo... |
ORPHA:354 |
Cardiac Valvular Dysplasia 1 |
|
Inguinal hernia, Hydroureter, Tricuspid regurgitation, Tricuspid stenosis, Edema, Valvular pulmon... |
OMIM:212093 |
Nephronophthisis 4 |
|
Polyuria, Stage 5 chronic kidney disease, Renal corticomedullary cysts, Nephronophthisis, Renal t... |
OMIM:606966 |
Alpha-Thalassemia |
|
Hydrops fetalis |
ORPHA:846 |
Exudative Vitreoretinopathy 6 |
|
Retinal detachment, Tractional retinal detachment, Patchy atrophy of the retinal pigment epitheli... |
OMIM:616468 |
Bartter Syndrome, Type 4B, Neonatal, With Sensorineural Deafness |
|
Hyperchloriduria, Fetal polyuria, Renal insufficiency, Premature birth, Polyuria, Polyhydramnios,... |
OMIM:613090 |
Donnai-Barrow Syndrome |
|
Omphalocele, Proteinuria, Congenital diaphragmatic hernia, Non-acidotic proximal tubulopathy, Umb... |
OMIM:222448 |
Short-Rib Thoracic Dysplasia 7 With Or Without Polydactyly |
|
Hypospadias, Hydrops fetalis, Renal cyst, Renal hypoplasia, Polycystic kidney dysplasia, Ascites |
OMIM:614091 |
Nephronophthisis 2 |
|
Absence of renal corticomedullary differentiation, Stage 5 chronic kidney disease, Hypertension, ... |
OMIM:602088 |
Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia |
|
Polyuria, Dehydration, Death in adolescence, Proximal tubulopathy, Death in childhood |
OMIM:560000 |
Fibrochondrogenesis 1 |
|
Omphalocele, Hydrops fetalis, Stillbirth, Camptodactyly, Joint contracture of the hand |
OMIM:228520 |
Lethal Congenital Contracture Syndrome 10 |
|
Omphalocele, Oligohydramnios, Hydrops fetalis, Fetal akinesia sequence |
OMIM:617022 |
Carpenter Syndrome 1 |
|
Omphalocele, Hydroureter, Pulmonic stenosis, Camptodactyly, Umbilical hernia, Joint contracture o... |
OMIM:201000 |
Fryns Syndrome |
|
Thickened nuchal skin fold, Omphalocele, Multicystic kidney dysplasia, Hypospadias, Polyhydramnio... |
ORPHA:2059 |
Focal Dermal Hypoplasia |
|
Omphalocele, Multicystic kidney dysplasia, Inguinal hernia, Telangiectasia of the skin, Abnormal ... |
ORPHA:2092 |
Schneckenbecken Dysplasia |
|
Umbilical hernia, Stillbirth, Nonimmune hydrops fetalis, Polyhydramnios |
OMIM:269250 |
Craniorachischisis |
|
Omphalocele, Congenital diaphragmatic hernia |
ORPHA:63260 |
Short-Rib Thoracic Dysplasia 12 |
|
Omphalocele, Inguinal hernia, Polyhydramnios, Edema, Renal hypoplasia, Neonatal death, Ascites, C... |
OMIM:269860 |
Cholestasis, Progressive Familial Intrahepatic, 5 |
|
Death in infancy, Pleural effusion, Ascites, Nonimmune hydrops fetalis |
OMIM:617049 |
Hemolytic Anemia Due To Red Cell Pyruvate Kinase Deficiency |
|
Hydrops fetalis |
ORPHA:766 |
Miller-Dieker Lissencephaly Syndrome |
|
Omphalocele, Decreased fetal movement, Inguinal hernia, Polyhydramnios, Abnormality of the abdomi... |
OMIM:247200 |
Coats Disease |
|
Exudative retinal detachment, Retinal telangiectasia |
OMIM:300216 |
Autosomal Recessive Polycystic Kidney Disease |
|
Gastrointestinal hemorrhage, Renal insufficiency, Recurrent urinary tract infections, Portal hype... |
ORPHA:731 |
Mucopolysaccharidosis, Type Vii |
|
Diastasis recti, Heparan sulfate excretion in urine, Flexion contracture, Hydrops fetalis, Dermat... |
OMIM:253220 |
Idiopathic Steroid-Sensitive Nephrotic Syndrome With Secondary Steroid Resistance |
|
Palpebral edema, Edema, Minimal change glomerulonephritis, Facial edema, Microscopic hematuria, P... |
ORPHA:567546 |
Mosaic Trisomy 9 |
|
Renal dysplasia, Hypoplasia of penis, Camptodactyly of finger, Polyhydramnios, Hydrops fetalis, H... |
ORPHA:99776 |
Thoracoabdominal Syndrome |
|
Omphalocele, Ventral hernia, Renal agenesis, Hypospadias, Congenital diaphragmatic hernia |
OMIM:313850 |
Lethal Omphalocele-Cleft Palate Syndrome |
|
Omphalocele |
ORPHA:2736 |
Melnick-Needles Syndrome |
|
Vesicoureteral reflux, Omphalocele, Hydronephrosis |
ORPHA:2484 |
Renal Dysplasia |
|
Abnormal renal calyx morphology, Urinary incontinence, Functional abnormality of the bladder, Ure... |
ORPHA:93108 |
Chromosome 9P Deletion Syndrome |
|
Omphalocele, Inguinal hernia, Hypospadias, Heart murmur, Micropenis |
OMIM:158170 |
Polycystic Kidney Disease 6 With Or Without Polycystic Liver Disease |
|
Renal insufficiency, Stage 5 chronic kidney disease, Hypertension, Polycystic kidney dysplasia, D... |
OMIM:618061 |
Radioulnar Synostosis With Amegakaryocytic Thrombocytopenia 2 |
|
Hydrops fetalis |
OMIM:616738 |
Osteogenesis Imperfecta, Type Ii |
|
Congestive heart failure, Pulmonary insufficiency, Premature birth, Nonimmune hydrops fetalis |
OMIM:166210 |
Capillary Malformation-Arteriovenous Malformation |
|
Neurogenic bladder, Nonimmune hydrops fetalis, Epistaxis, Lymphedema, High-output congestive hear... |
ORPHA:137667 |
Dyssegmental Dysplasia, Silverman-Handmaker Type |
|
Miscarriage, Flexion contracture, Hydrops fetalis, Single umbilical artery, Increased placental t... |
ORPHA:1865 |
Hennekam Lymphangiectasia-Lymphedema Syndrome 1 |
|
Nonimmune hydrops fetalis, Lymphedema, Periorbital edema, Pericardial effusion, Ectopic kidney, H... |
OMIM:235510 |
Senior-Loken Syndrome 1 |
|
Renal insufficiency, Polyuria, Thickening of the tubular basement membrane, Impaired renal concen... |
OMIM:266900 |
Developmental Delay With Or Without Dysmorphic Facies And Autism |
|
Omphalocele, Inguinal hernia, Congenital diaphragmatic hernia, Renal hypoplasia, Renal cyst, Pulm... |
OMIM:618454 |
Beckwith-Wiedemann Syndrome |
|
Omphalocele, Diastasis recti, Nephrolithiasis, Renal cortical cysts, Nephrocalcinosis, Cardiomyop... |
OMIM:130650 |
Hypotrichosis-Lymphedema-Telangiectasia Syndrome |
|
Palmar telangiectasia, Predominantly lower limb lymphedema, Nonimmune hydrops fetalis, Palpebral ... |
OMIM:607823 |
Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease |
|
Renal insufficiency, Portal hypertension, Absence of renal corticomedullary differentiation, Hema... |
OMIM:263200 |
Short-Rib Thoracic Dysplasia 19 With Or Without Polydactyly |
|
Omphalocele |
OMIM:617895 |
Simpson-Golabi-Behmel Syndrome |
|
Omphalocele, Ureteral duplication, Hypoplasia of penis, Multicystic kidney dysplasia, Hypospadias... |
ORPHA:373 |
Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins |
|
Thickened nuchal skin fold, Omphalocele, Hydroureter, Hypospadias, Nonimmune hydrops fetalis, Pol... |
OMIM:265380 |
Alg9-Cdg |
|
Thickened nuchal skin fold, Decreased fetal movement, Omphalocele, Tricuspid regurgitation, Lipod... |
ORPHA:79328 |
Gm1 Gangliosidosis Type 1 |
|
Hydrops fetalis, Cardiomyopathy, Urinary glycosaminoglycan excretion, Abnormal odontoid tissue mo... |
ORPHA:79255 |
Hypomagnesemia, Seizures, And Impaired Intellectual Development 2 |
|
Renal magnesium wasting, Nephrocalcinosis, Polyuria, Renal potassium wasting |
OMIM:618314 |
Acrocephalopolydactylous Dysplasia |
|
Omphalocele, Ascites, Cystic renal dysplasia, Enlarged kidney |
OMIM:200995 |
Chromosome 10Q26 Deletion Syndrome |
|
Vesicoureteral reflux, Micropenis, Omphalocele |
OMIM:609625 |
Platyspondylic Dysplasia, Torrance Type |
|
Hydrops fetalis, Polyhydramnios |
ORPHA:85166 |
Senior-Loken Syndrome 3 |
|
Polyuria, Stage 5 chronic kidney disease, Enuresis, Renal corticomedullary cysts, Nephronophthisis |
OMIM:606995 |
Growth Delay-Hydrocephaly-Lung Hypoplasia Syndrome |
|
Omphalocele |
ORPHA:3035 |
Multicentric Osteolysis-Nodulosis-Arthropathy Spectrum |
|
Omphalocele, Hypertension, Atrioventricular block |
ORPHA:371428 |
Amelogenesis Imperfecta, Type Ig |
|
Renal insufficiency, Polyuria, Impaired renal concentrating ability, Nephrocalcinosis, Enuresis, ... |
OMIM:204690 |
Gaucher Disease, Perinatal Lethal |
|
Decreased fetal movement, Premature birth, Nonimmune hydrops fetalis, Polyhydramnios, Desquamatio... |
OMIM:608013 |
Achondrogenesis, Type Ia |
|
Polyhydramnios, Increased nuchal translucency, Hydrops fetalis, Stillbirth, Absence of stomach bu... |
OMIM:200600 |
Type 1 Diabetes Mellitus |
|
Polyuria |
OMIM:222100 |
Hyperuricemia, Pulmonary Hypertension, Renal Failure, And Alkalosis Syndrome |
|
Proteinuria, Premature birth, Polyuria, Renal salt wasting, Chronic kidney disease, Pulmonary art... |
OMIM:613845 |
Constricting Bands, Congenital |
|
Omphalocele, Bladder exstrophy, Gastroschisis |
OMIM:217100 |
Cardiac Diverticulum |
|
Omphalocele, Abnormal EKG, Mitral stenosis, Diastasis recti, Angina pectoris, Tricuspid stenosis,... |
ORPHA:1686 |
Pagod Syndrome |
|
Omphalocele, Death in infancy, Multicystic kidney dysplasia, Sudden cardiac death, Congenital dia... |
ORPHA:991 |
Multiple Pterygium Syndrome, Escobar Variant |
|
Decreased fetal movement, Inguinal hernia, Multiple joint contractures, Hypospadias, Congenital d... |
OMIM:265000 |
Hyperaldosteronism, Familial, Type Iii |
|
Hypercalciuria, Hypertension, Polyuria |
OMIM:613677 |
Medium Chain 3-Ketoacyl-Coa Thiolase Deficiency |
|
Neonatal death, Myoglobinuria, Dehydration |
OMIM:602199 |
Combined Oxidative Phosphorylation Deficiency 41 |
|
Premature birth, Nonimmune hydrops fetalis |
OMIM:618838 |
Developmental And Epileptic Encephalopathy 89 |
|
Neonatal death, Flexion contracture, Omphalocele, Death in childhood |
OMIM:619124 |
Pentalogy Of Cantrell |
|
Omphalocele, Renal agenesis, Hypospadias, Congenital diaphragmatic hernia, Renal dysplasia |
ORPHA:1335 |
Hypomagnesemia 3, Renal |
|
Recurrent urinary tract infections, Polyuria, Hypocitraturia, Renal magnesium wasting, Chronic ki... |
OMIM:248250 |
Teebi Hypertelorism Syndrome 1 |
|
Omphalocele, Single umbilical artery |
OMIM:145420 |
Oligomeganephronia |
|
Renal insufficiency, Premature birth, Proteinuria, Unilateral renal agenesis, Congenital diaphrag... |
ORPHA:2260 |
Holoprosencephaly-Postaxial Polydactyly Syndrome |
|
Omphalocele, Hypoplasia of penis, Hypospadias, Polyhydramnios, Renal hypoplasia/aplasia, Abnormal... |
ORPHA:2166 |
Methylmalonic Acidemia With Homocystinuria, Type Cblc |
|
Glomerulopathy, Renal insufficiency, Ketonuria, Pulmonary embolism, Hemolytic-uremic syndrome, Di... |
ORPHA:79282 |
Robinow Syndrome, Autosomal Recessive 2 |
|
Ventral hernia, Omphalocele, Camptodactyly |
OMIM:618529 |
Exercise-Induced Malignant Hyperthermia |
|
Prolonged QT interval, Sinus tachycardia, Oliguria, ST segment depression, Hypotension, Abnormal ... |
ORPHA:466650 |
Beckwith-Wiedemann Syndrome |
|
Omphalocele, Ureteral duplication, Inguinal hernia, Premature birth, Diastasis recti, Polyhydramn... |
ORPHA:116 |
C Syndrome |
|
Omphalocele, Renal cortical cysts |
OMIM:211750 |
Kagami-Ogata Syndrome |
|
Omphalocele, Inguinal hernia, Premature birth, Diastasis recti, Polyhydramnios, Large placenta |
ORPHA:254519 |
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 |
|
Duplicated collecting system, Death in infancy, Hip contracture, Bilateral fetal pyelectasis, Pol... |
OMIM:300868 |
Trisomy 18 |
|
Omphalocele, Camptodactyly of finger, Congenital diaphragmatic hernia, Abnormality of the upper u... |
ORPHA:3380 |
Fryns Syndrome |
|
Omphalocele, Ureteral duplication, Hypospadias, Renal agenesis, Polyhydramnios, Renal cyst, Still... |
OMIM:229850 |
Tibial Aplasia-Ectrodactyly Syndrome |
|
Omphalocele |
ORPHA:3329 |
Pseudotrisomy 13 Syndrome |
|
Omphalocele, Micropenis, Renal agenesis, Renal hypoplasia |
OMIM:264480 |
Short-Rib Thoracic Dysplasia 14 With Polydactyly |
|
Congenital diaphragmatic hernia, Polyhydramnios, Hydrops fetalis, Polycystic kidney dysplasia, Mi... |
OMIM:616546 |
Diarrhea 10, Protein-Losing Enteropathy Type |
|
Death in infancy, Polyuria, Polyhydramnios, Pericardial effusion, Hematochezia, Anasarca, Pleural... |
OMIM:618183 |
S-Adenosylhomocysteine Hydrolase Deficiency |
|
Cardiomyopathy, Hydrops fetalis |
ORPHA:88618 |
Ifap Syndrome 1, With Or Without Bresheck Syndrome |
|
Omphalocele, Death in infancy, Multicystic kidney dysplasia, Inguinal hernia, Hypospadias, Renal ... |
OMIM:308205 |
Lymphedema-Distichiasis Syndrome |
|
Predominantly lower limb lymphedema, Nonimmune hydrops fetalis, Lymphedema, Chylothorax, Cellulit... |
OMIM:153400 |
D-Lactic Aciduria With Gout |
|
Inguinal hernia |
OMIM:245450 |
Short-Rib Thoracic Dysplasia 13 With Or Without Polydactyly |
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Omphalocele, Stillbirth, Renal hypoplasia, Renal cyst |
OMIM:616300 |
Denys-Drash Syndrome |
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Diffuse mesangial sclerosis, Posterolateral diaphragmatic hernia, Congenital diaphragmatic hernia... |
OMIM:194080 |
Pearson Marrow-Pancreas Syndrome |
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Hydrops fetalis, Dehydration, Hypercalciuria, 3-Methylglutaric aciduria, Renal Fanconi syndrome, ... |
OMIM:557000 |
Nephronophthisis 11 |
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Tubular basement membrane disintegration, Polyuria, Stage 5 chronic kidney disease, Renal cortico... |
OMIM:613550 |
Congenital Myopathy 22B, Severe Fetal |
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Decreased fetal movement, Hip contracture, Limb joint contracture, Nonimmune hydrops fetalis, Pol... |
OMIM:620369 |
Mycophenolate Mofetil Embryopathy |
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Hydrops fetalis, Congenital diaphragmatic hernia, Ectopic kidney |
ORPHA:268249 |
Immunodeficiency 80 With Or Without Congenital Cardiomyopathy |
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Pericardial effusion, Restrictive cardiomyopathy, Nonimmune hydrops fetalis |
OMIM:619313 |
Greenberg Dysplasia |
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Nonimmune hydrops fetalis, Polyhydramnios, Echogenic fetal bowel, Large placenta, Increased nucha... |
OMIM:215140 |
Opitz Gbbb Syndrome |
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Omphalocele, Inguinal hernia, Hypospadias, Congenital diaphragmatic hernia, Abnormality of the ur... |
ORPHA:2745 |
Otopalatodigital Syndrome, Type I |
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Omphalocele |
OMIM:311300 |
Farber Disease |
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Joint swelling, Ascites, Flexion contracture, Hydrops fetalis |
ORPHA:333 |
Diabetes Insipidus, Nephrogenic, 2, Autosomal |
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Megacystis, Polyuria, Hypertonic dehydration |
OMIM:125800 |
Diabetes Insipidus, Nephrogenic, 1, X-Linked |
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Megacystis, Polyuria, Hypertonic dehydration |
OMIM:304800 |
Bartter Syndrome, Type 1, Antenatal |
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Hyperchloriduria, Fetal polyuria, Premature birth, Polyuria, Polyhydramnios, Renal salt wasting, ... |
OMIM:601678 |
Alport Syndrome 3A, Autosomal Dominant |
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Renal insufficiency, Glomerular basement membrane lamellation, Proteinuria, Glomerulonephritis, S... |
OMIM:104200 |
Anemia, Congenital Dyserythropoietic, Type Iv |
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Hypertrophic cardiomyopathy, Micropenis, Hypospadias, Hydrops fetalis |
OMIM:613673 |
Hennekam Syndrome |
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Camptodactyly of finger, Lymphedema, Pericardial effusion, Ectopic kidney, Hydrops fetalis, Horse... |
ORPHA:2136 |
Robinow Syndrome, Autosomal Dominant 3 |
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Omphalocele, Tricuspid regurgitation, Camptodactyly, Vesicoureteral reflux, Micropenis |
OMIM:616894 |
Galactosialidosis |
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Conjunctival telangiectasia, Nonimmune hydrops fetalis |
OMIM:256540 |
Osteopathia Striata With Cranial Sclerosis |
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Omphalocele, Multicystic kidney dysplasia, Polyhydramnios, Camptodactyly, Joint contracture of th... |
OMIM:300373 |
Oeis Complex |
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Omphalocele, Duplicated collecting system, Hydroureter, Renal agenesis, Epispadias, Vesicovaginal... |
OMIM:258040 |
Gitelman Syndrome |
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Prolonged QT interval, Polyuria, Renal magnesium wasting, Ventricular tachycardia, Enuresis, Hypo... |
OMIM:263800 |
Manitoba Oculotrichoanal Syndrome |
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Omphalocele |
OMIM:248450 |
Fibrochondrogenesis |
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Omphalocele, Camptodactyly of finger |
ORPHA:2021 |
Gaucher Disease Type 3 |
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Proteinuria, Pericardial effusion, Hydrops fetalis, Hematuria, Pulmonary arterial hypertension |
ORPHA:77261 |
3Mc Syndrome 1 |
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Omphalocele, Conjunctival telangiectasia, Diastasis recti, Abnormality of the abdominal wall, Hyd... |
OMIM:257920 |
Melnick-Needles Syndrome |
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Omphalocele, Ureteral stenosis, Stillbirth, Pulmonary arterial hypertension, Hydronephrosis |
OMIM:309350 |
Cranioectodermal Dysplasia 2 |
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Inguinal hernia, Renal insufficiency, Polyhydramnios, Hydrops fetalis, Renal cyst, Hypertension |
OMIM:613610 |
Otopalatodigital Syndrome Type 2 |
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Omphalocele, Hypospadias, Camptodactyly of finger, Ureteral obstruction, Hydronephrosis |
ORPHA:90652 |
Fetal Akinesia Deformation Sequence 1 |
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Decreased fetal movement, Hip contracture, Premature birth, Nonimmune hydrops fetalis, Polyhydram... |
OMIM:208150 |
Bartsocas-Papas Syndrome 1 |
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Omphalocele, Decreased fetal movement, Inguinal hernia, Ectopic kidney, Flexion contracture, Arth... |
OMIM:263650 |
Iniencephaly |
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Omphalocele, Renal agenesis, Congenital diaphragmatic hernia, Polyhydramnios, Gastroschisis, Arth... |
ORPHA:63259 |
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 3 |
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Hydroureter, Polyhydramnios, Megacystis, Fetal megacystis, Neonatal death, Hydronephrosis |
OMIM:619362 |
Pearson Syndrome |
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Renal insufficiency, Proteinuria, Cardiac conduction abnormality, Hydrops fetalis, Renal cyst, De... |
ORPHA:699 |
C Syndrome |
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Omphalocele, Death in infancy, Multicystic kidney dysplasia, Congenital diaphragmatic hernia, Pol... |
ORPHA:1308 |
Marshall-Smith Syndrome |
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Omphalocele, Premature ventricular contraction, Pulmonary arterial hypertension, Hypertension, De... |
OMIM:602535 |
Mgat2-Cdg |
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Arrhythmia, Hydrops fetalis, Reflex asystolic syncope |
ORPHA:79329 |
Meckel Syndrome, Type 1 |
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Omphalocele, Hypoplasia of the bladder, Renal agenesis, Camptodactyly of finger, Breech presentat... |
OMIM:249000 |
Seizures, Sensorineural Deafness, Ataxia, Impaired Intellectual Development, And Electrolyte Imbalance |
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Polyuria, Renal salt wasting, Enuresis, Hypertension, Hypocalciuria, Renal sodium wasting, Renal ... |
OMIM:612780 |
Holoprosencephaly |
|
Omphalocele, Hypoplasia of penis, Proteinuria, Congenital diaphragmatic hernia, Abnormality of th... |
ORPHA:2162 |
Bartter Syndrome, Type 2, Antenatal |
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Hyperchloriduria, Fetal polyuria, Premature birth, Polyuria, Polyhydramnios, Renal salt wasting, ... |
OMIM:241200 |
Short-Rib Thoracic Dysplasia 6 With Or Without Polydactyly |
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Micropenis, Tricuspid regurgitation, Hydrops fetalis, Polycystic kidney dysplasia |
OMIM:263520 |
Myoectodermal Gonadal Dysgenesis Syndrome |
|
Omphalocele, Diastasis recti, Unilateral renal agenesis |
OMIM:618419 |
Helix Syndrome |
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Renal insufficiency, Polyuria, Xerostomia, Nephrolithiasis, Hypocalciuria |
OMIM:617671 |
Bardet-Biedl Syndrome 17 |
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Polyuria, Micropenis, Stage 5 chronic kidney disease, Renal cyst |
OMIM:615994 |
Bladder Exstrophy And Epispadias Complex |
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Inguinal hernia, Hydroureter, Unilateral renal agenesis, Epispadias, Horseshoe kidney, Bladder ex... |
OMIM:600057 |
Generalized Arterial Calcification Of Infancy |
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Hyperphosphaturia, Transient ischemic attack, Left ventricular systolic dysfunction, Polyhydramni... |
ORPHA:51608 |
Heterotaxy, Visceral, 1, X-Linked |
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Omphalocele, Renal agenesis, Polyhydramnios, Horseshoe kidney, Pulmonic stenosis, Mitral stenosis... |
OMIM:306955 |
Esophageal Atresia |
|
Omphalocele, Renal agenesis, Polyhydramnios, Abnormality of the urinary system, Absence of stomac... |
ORPHA:1199 |
Codas Syndrome |
|
Omphalocele, Enamel hypoplasia, Polyhydramnios |
OMIM:600373 |
Hepatoerythropoietic Porphyria |
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Nonimmune hydrops fetalis, Edema, Scarring, Scarring alopecia of scalp, Red-brown urine, Red urin... |
ORPHA:95159 |
Autoimmune Lymphoproliferative Syndrome |
|
Renal insufficiency, Glomerulonephritis, Vasculitis, Hydrops fetalis, Panniculitis |
ORPHA:3261 |
Teratoma, Pineal |
|
Polyuria |
OMIM:273120 |
Specc1L-Related Hypertelorism Syndrome |
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Omphalocele, Umbilical hernia, Arrhythmia, Ectopic kidney |
ORPHA:1519 |
Anemia, Congenital Dyserythropoietic, Type Ia |
|
Hydrops fetalis |
OMIM:224120 |
Okamoto Syndrome |
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Omphalocele, Urinary incontinence, Unilateral renal hypoplasia, Aortic valve stenosis, Ureteropel... |
ORPHA:2729 |
Gaucher Disease |
|
Death in infancy, Proteinuria, Hydrops fetalis, Hematuria, Pulmonary arterial hypertension, Arthr... |
ORPHA:355 |
Ablepharon-Macrostomia Syndrome |
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Ventral hernia, Omphalocele, Single umbilical artery, Camptodactyly, Absent lanugo, Micropenis |
OMIM:200110 |
Combined Immunodeficiency-Enteropathy Spectrum |
|
Omphalocele, Congenital pulmonary airway malformation, Polyhydramnios |
ORPHA:436252 |
Yunis-Varon Syndrome |
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Hypospadias, Polyhydramnios, Increased nuchal translucency, Hydrops fetalis, Renovascular hyperte... |
ORPHA:3472 |
Pyruvate Kinase Deficiency Of Red Cells |
|
Nonimmune hydrops fetalis |
OMIM:266200 |
Kagami-Ogata Syndrome Due To Paternal Uniparental Disomy Of Chromosome 14 |
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Omphalocele, Miscarriage, Premature birth, Polyhydramnios, Interphalangeal joint contracture of f... |
ORPHA:96334 |
Hydrolethalus Syndrome 1 |
|
Omphalocele, Hypospadias, Polyhydramnios, Stillbirth, Hydronephrosis |
OMIM:236680 |
Arima Syndrome |
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Proteinuria, Polyuria, Stage 5 chronic kidney disease, Hematuria, Hypertension, Renal corticomedu... |
OMIM:243910 |
Focal Dermal Hypoplasia |
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Omphalocele, Ureteral duplication, Inguinal hernia, Diastasis recti, Congenital diaphragmatic her... |
OMIM:305600 |
Ablepharon Macrostomia Syndrome |
|
Omphalocele, Umbilical hernia, Hypoplasia of penis, Camptodactyly of finger |
ORPHA:920 |
Congenital Erythropoietic Porphyria |
|
Nonimmune hydrops fetalis, Edema, Scarring, Increased connective tissue, Scarring alopecia of sca... |
ORPHA:79277 |
Blomstrand Lethal Chondrodysplasia |
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Premature birth, Hydrops fetalis, Polyhydramnios |
ORPHA:50945 |
Phocomelia, Schinzel Type |
|
Hypoplasia of penis, Hydrops fetalis |
ORPHA:2879 |
Hereditary Elliptocytosis |
|
Hydrops fetalis |
ORPHA:288 |
Genitourinary And/Or Brain Malformation Syndrome |
|
Omphalocele, Hypospadias, Chordee, Micropenis, Urogenital sinus anomaly |
OMIM:618820 |
Fraser Syndrome |
|
Omphalocele, Death in infancy, Hypoplasia of penis, Multicystic kidney dysplasia, Hypospadias, Re... |
ORPHA:2052 |
Holoprosencephaly-Radial Heart Renal Anomalies Syndrome |
|
Omphalocele, Abnormal localization of kidney, Renal hypoplasia/aplasia |
ORPHA:3186 |
Short Rib-Polydactyly Syndrome, Verma-Naumoff Type |
|
Omphalocele, Hypoplasia of penis, Urethrovaginal fistula, Hydrops fetalis, Renal cyst, Renal hypo... |
ORPHA:93271 |
Shprintzen Omphalocele Syndrome |
|
Omphalocele, Single umbilical artery |
OMIM:182210 |
Sacral Agenesis With Vertebral Anomalies |
|
Neonatal death, Unilateral renal agenesis, Persistent cloaca |
OMIM:615709 |
Ichthyosis Follicularis-Alopecia-Photophobia Syndrome |
|
Omphalocele, Inguinal hernia, Hydroureter, Abnormal dental enamel morphology, Camptodactyly of fi... |
ORPHA:2273 |
Cystinosis, Nephropathic |
|
Renal insufficiency, Hyperphosphaturia, Proteinuria, Polyuria, Stage 5 chronic kidney disease, De... |
OMIM:219800 |
Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 |
|
Decreased renal tubular phosphate excretion, Nephrocalcinosis, Enamel hypoplasia, Increased renal... |
OMIM:211900 |
Omphalocele Syndrome, Shprintzen-Goldberg Type |
|
Omphalocele |
ORPHA:3164 |
Hyperparathyroidism, Neonatal Severe |
|
Polyuria, Aminoaciduria, Hyperphosphaturia, Hypercalciuria |
OMIM:239200 |
Niemann-Pick Disease Type C |
|
Aplasia/Hypoplasia of the abdominal wall musculature, Ascites, Hydrops fetalis, Fetal ascites |
ORPHA:646 |
Otopalatodigital Syndrome, Type Ii |
|
Omphalocele, Hypospadias, Elbow contracture, Stillbirth, Umbilical hernia, Hydronephrosis |
OMIM:304120 |
Charge Syndrome |
|
Omphalocele, Renal agenesis, Polyhydramnios, Renal hypoplasia, Horseshoe kidney, Pulmonic stenosi... |
OMIM:214800 |
Diamond-Blackfan Anemia |
|
Renal agenesis, Hypospadias, Nonimmune hydrops fetalis, Horseshoe kidney |
ORPHA:124 |
Holoprosencephaly 7 |
|
Omphalocele |
OMIM:610828 |
Lipodystrophy, Familial Partial, Type 7 |
|
Loss of subcutaneous adipose tissue in limbs, Reduced subcutaneous adipose tissue, Orthostatic hy... |
OMIM:606721 |
Pallister-Killian Syndrome |
|
Omphalocele, Inguinal hernia, Edema of the dorsum of feet, Hypospadias, Polyhydramnios, Congenita... |
OMIM:601803 |
Zttk Syndrome |
|
Aortic regurgitation, Polyuria, Unilateral renal agenesis, Breech presentation, Flexion contractu... |
OMIM:617140 |
Yunis-Varon Syndrome |
|
Hypospadias, Premature birth, Polyhydramnios, Hydrops fetalis, Heart murmur, Cardiomyopathy, Pulm... |
OMIM:216340 |
Autosomal Recessive Hypophosphatemic Rickets |
|
Renal phosphate wasting, Hyperphosphaturia, Abnormality of renal excretion, Enthesitis |
ORPHA:289176 |
Young-Onset Parkinson Disease |
|
|
ORPHA:2828 |
Atypical Juvenile Parkinsonism |
|
|
ORPHA:391411 |