| Schizophrenia 15 |
|
Hyperactivity |
OMIM:613950 |
| Attention Deficit-Hyperactivity Disorder |
|
Attention deficit hyperactivity disorder, Hyperactivity |
OMIM:143465 |
| Attention Deficit-Hyperactivity Disorder 8 |
|
Attention deficit hyperactivity disorder |
OMIM:619957 |
| 22q13 deletion syndrome (Phelan-Mcdermid syndrome) |
|
Hyperactivity |
DECIPHER:20 |
| Autism, Susceptibility To, X-Linked 4 |
|
Aggressive behavior, Attention deficit hyperactivity disorder, Motor tics, Impulsivity |
OMIM:300830 |
| Attention Deficit-Hyperactivity Disorder, Susceptibility To, 7 |
|
Attention deficit hyperactivity disorder |
OMIM:613003 |
| Gilles De La Tourette Syndrome |
|
Phonic tics, Self-mutilation, Aggressive behavior, Attention deficit hyperactivity disorder, Moto... |
OMIM:137580 |
| Potocki-Lupski syndrome (17p11.2 duplication syndrome) |
|
Hyperactivity |
DECIPHER:19 |
| Autism, Susceptibility To, 20 |
|
Compulsive behaviors, Attention deficit hyperactivity disorder |
OMIM:618830 |
| Intellectual Developmental Disorder, Autosomal Recessive 3 |
|
Hyperactivity |
OMIM:608443 |
| Intellectual Developmental Disorder, Autosomal Recessive 2 |
|
Self-injurious behavior, Attention deficit hyperactivity disorder |
OMIM:607417 |
| Intellectual Developmental Disorder, X-Linked 77 |
|
Hyperactivity |
OMIM:300454 |
| Intellectual Developmental Disorder, Autosomal Recessive 37 |
|
Bruxism, Aggressive behavior, Hyperactivity |
OMIM:615493 |
| Ank3-Related Intellectual Disability-Sleep Disturbance Syndrome |
|
Bruxism, Aggressive behavior, Hyperactivity |
ORPHA:356996 |
| Smith-Magenis syndrome |
|
Motor stereotypy, Hyperactivity, Self-mutilation |
DECIPHER:8 |
| Intellectual Developmental Disorder, X-Linked 72 |
|
Motor stereotypy, Hyperactivity |
OMIM:300271 |
| Intellectual Developmental Disorder, X-Linked 109 |
|
Stereotypical body rocking, Recurrent hand flapping, Agitation, Aggressive behavior, Hyperactivit... |
OMIM:309548 |
| Fraxe Intellectual Disability |
|
Stereotypical body rocking, Recurrent hand flapping, Impulsivity, Aggressive behavior, Hyperactiv... |
ORPHA:100973 |
| Intellectual Developmental Disorder, Autosomal Dominant 33 |
|
Hyperactivity |
OMIM:616311 |
| Intellectual Developmental Disorder, X-Linked, Syndromic, Houge Type |
|
Attention deficit hyperactivity disorder, Hyperactivity, Impulsivity |
OMIM:301008 |
| Intellectual Developmental Disorder With Epilepsy, Behavioral Abnormalities, And Coarse Facies |
|
Self-injurious behavior, Aggressive behavior, Hyperactivity |
OMIM:619031 |
| Pick Disease Of Brain |
|
Inappropriate laughter, Disinhibition, Irritability, Polyphagia, Emotional blunting, Motor stereo... |
OMIM:172700 |
| Progressive Non-Fluent Aphasia |
|
Mental deterioration, Temporal cortical atrophy, Frontotemporal cerebral atrophy, Memory impairme... |
ORPHA:100070 |
| Megalencephalic Leukoencephalopathy With Subcortical Cysts 4, Remitting |
|
Dysphagia, Hyperactivity, Impulsivity |
OMIM:620448 |
| Obesity Due To Sim1 Deficiency |
|
Hypotension, Postural hypotension with compensatory tachycardia, Polyphagia, Attention deficit hy... |
ORPHA:369873 |
| Intellectual Developmental Disorder, X-Linked, Syndromic, Pilorge Type |
|
Hyperactivity, Inflexible adherence to routines |
OMIM:301076 |
| Intellectual Disability-Expressive Aphasia-Facial Dysmorphism Syndrome |
|
Hyperactivity |
ORPHA:436151 |
| Developmental And Epileptic Encephalopathy 104 |
|
Self-injurious behavior, Hyperactivity, Agitation |
OMIM:619970 |
| Sporadic Creutzfeldt-Jakob Disease |
|
Memory impairment, Cerebral atrophy, Confusion, Astrocytosis, Cognitive impairment, Neuronal loss... |
ORPHA:204 |
| Obesity Due To Melanocortin 4 Receptor Deficiency |
|
Polyphagia, Hypertension |
ORPHA:71529 |
| Pandas |
|
Depression, Abnormal fear-induced behavior, Oppositional defiant disorder, Obsessive-compulsive t... |
ORPHA:66624 |
| Frontotemporal Dementia |
|
Polyphagia, Inappropriate laughter, Irritability, Disinhibition |
OMIM:600274 |
| Kleine-Levin Syndrome |
|
Depression, Polydipsia, Abnormal eating behavior, Irritability, Sweet craving, Polyphagia, Repeti... |
ORPHA:33543 |
| Developmental And Epileptic Encephalopathy 43 |
|
Attention deficit hyperactivity disorder, Hyperactivity, Impulsivity |
OMIM:617113 |
| Severe Early-Onset Obesity-Insulin Resistance Syndrome Due To Sh2B1 Deficiency |
|
Aggressive behavior, Polyphagia |
ORPHA:329249 |
| Huntington Disease |
|
Depression, Oral-pharyngeal dysphagia, Hostility, Irritability, Disinhibition, Polyphagia, Addict... |
ORPHA:399 |
| Kleine-Levin Hibernation Syndrome |
|
Polyphagia |
OMIM:148840 |
| Focal Cortical Dysplasia, Type Ii |
|
Astrocytosis, Cognitive impairment |
OMIM:607341 |
| Obesity, Hyperphagia, And Developmental Delay |
|
Polyphagia, Motor stereotypy |
OMIM:613886 |
| Hyperprolinemia, Type I |
|
Aggressive behavior, Motor stereotypy, Hyperactivity |
OMIM:239500 |
| Glycine Encephalopathy 1 |
|
Aggressive behavior, Restlessness, Hyperactivity, Impulsivity |
OMIM:605899 |
| Intellectual Developmental Disorder, X-Linked 111 |
|
Phonic tics, Aggressive behavior, Hyperactivity, Compulsive behaviors |
OMIM:301107 |
| Hyperinsulinism Due To Ucp2 Deficiency |
|
Hypertrophic cardiomyopathy, Palpitations, Polyphagia, Syncope, Tachycardia, Agitation |
ORPHA:276556 |
| Morm Syndrome |
|
Aggressive behavior, Hyperactivity |
ORPHA:75858 |
| Intellectual Developmental Disorder, Autosomal Dominant 67 |
|
Compulsive behaviors, Attention deficit hyperactivity disorder, Motor tics, Hyperactivity |
OMIM:619927 |
| Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency |
|
Hypertrophic cardiomyopathy, Palpitations, Polyphagia, Syncope, Tachycardia, Agitation |
ORPHA:276575 |
| Intellectual Developmental Disorder, Autosomal Dominant 39 |
|
Polyphagia, Aggressive behavior, Self-mutilation |
OMIM:616521 |
| Hartnup Disorder |
|
Attention deficit hyperactivity disorder, Hyperactivity |
OMIM:234500 |
| Graves Disease |
|
Polyphagia, Congestive heart failure, Hyperactivity, Irritability |
OMIM:275000 |
| Bilateral Parasagittal Parieto-Occipital Polymicrogyria |
|
Aggressive behavior, Abnormal fear-induced behavior, Pseudobulbar paralysis |
ORPHA:208441 |
| Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency |
|
Hypertrophic cardiomyopathy, Palpitations, Polyphagia, Syncope, Tachycardia, Agitation |
ORPHA:276580 |
| Leptin Receptor Deficiency |
|
Aggressive behavior, Polyphagia, Abnormal eating behavior, Emotional lability |
OMIM:614963 |
| Body Mass Index Quantitative Trait Locus 20 |
|
Polyphagia |
OMIM:618406 |
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7 |
|
Cerebral cortical atrophy, Memory impairment, Astrocytosis, Frontotemporal dementia, Neuronal los... |
OMIM:600795 |
| Hyperinsulinism Due To Hnf1A Deficiency |
|
Palpitations, Polyphagia, Syncope, Tachycardia, Agitation |
ORPHA:324575 |
| Obesity And Hypopigmentation |
|
Polyphagia |
OMIM:620195 |
| 8p23.1 deletion syndrome |
|
Hyperactivity |
DECIPHER:39 |
| 14Q11.2 Microduplication Syndrome |
|
Polyphagia, Attention deficit hyperactivity disorder, Aggressive behavior |
ORPHA:261229 |
| Type 1 Diabetes Mellitus |
|
Polyphagia, Polydipsia |
OMIM:222100 |
| Bardet-Biedl Syndrome 22 |
|
Polyphagia |
OMIM:617119 |
| Angelman Syndrome Due To Imprinting Defect In 15Q11-Q13 |
|
Polyphagia, Inappropriate laughter, Hyperactivity |
ORPHA:411515 |
| Leptin Deficiency Or Dysfunction |
|
Polyphagia |
OMIM:614962 |
| Renal Glucosuria |
|
Polyphagia, Polydipsia |
OMIM:233100 |
| X-Linked Intellectual Disability-Psychosis-Macroorchidism Syndrome |
|
Abnormal fear-induced behavior, Congestive heart failure, Irritability, Aggressive behavior, Hype... |
ORPHA:3077 |
| 2Q23.1 Microdeletion Syndrome |
|
Self-injurious behavior, Polyphagia, Motor stereotypy, Hyperactivity, Paroxysmal bursts of laughter |
ORPHA:228402 |
| Female Restricted Epilepsy With Intellectual Disability |
|
Abnormal eating behavior, Aggressive behavior, Hyperactivity, Compulsive behaviors, Impulsivity |
ORPHA:101039 |
| Intellectual Developmental Disorder, Autosomal Recessive 75, With Neuropsychiatric Features And Variant Lissencephaly |
|
Self-injurious behavior, Inappropriate behavior, Aggressive behavior, Attention deficit hyperacti... |
OMIM:619827 |
| Hypotonia-Cystinuria Syndrome |
|
Polyphagia |
ORPHA:163690 |
| Inherited Creutzfeldt-Jakob Disease |
|
Central nervous system degeneration, Global brain atrophy, Confusion, Chorea, Astrocytosis, Gait ... |
ORPHA:282166 |
| Pediatric-Onset Graves Disease |
|
Polydipsia, Sinus tachycardia, Congestive heart failure, Palpitations, Emotional lability, Irrita... |
ORPHA:525731 |
| Wagro Syndrome |
|
Low frustration tolerance, Emotional lability, Polyphagia, Aggressive behavior, Compulsive behavi... |
OMIM:612469 |
| Lodder-Merla Syndrome, Type 2, With Developmental Delay And With Or Without Cardiac Arrhythmia |
|
Attention deficit hyperactivity disorder, Hyperactivity |
OMIM:617182 |
| 6Q16 Microdeletion Syndrome |
|
Abnormal temper tantrums, Polyphagia |
ORPHA:171829 |
| Prader-Willi Syndrome Due To Imprinting Mutation |
|
Polyphagia |
ORPHA:177910 |
| Behavioral Variant Of Frontotemporal Dementia |
|
Mental deterioration, Memory impairment, Frontotemporal cerebral atrophy, Astrocytosis, Frontotem... |
ORPHA:275864 |
| Hypermetabolism Due To Uncoupled Mitochondrial Oxidative Phosphorylation 2 |
|
Polyphagia |
OMIM:620085 |
| Intellectual Developmental Disorder, Autosomal Dominant 72 |
|
Polyphagia, Attention deficit hyperactivity disorder, Overfriendliness |
OMIM:620439 |
| Obesity Due To Prohormone Convertase I Deficiency |
|
Polyphagia |
ORPHA:71528 |
| Obesity Due To Pro-Opiomelanocortin Deficiency |
|
Polyphagia |
ORPHA:71526 |
| Intellectual Developmental Disorder, Autosomal Recessive 38 |
|
Aggressive behavior, Recurrent hand flapping, Hyperactivity, Self-mutilation |
OMIM:615516 |
| Chromosome 22Q13 Duplication Syndrome |
|
Polyphagia, Attention deficit hyperactivity disorder, Emotional lability, Impulsivity |
OMIM:615538 |
| Joubert Syndrome 10 |
|
Polyphagia, Frequent temper tantrums |
OMIM:300804 |
| Trisomy 18P |
|
Polyphagia, Attention deficit hyperactivity disorder, Facial palsy |
ORPHA:1715 |
| Familial Infantile Bilateral Striatal Necrosis |
|
Astrocytosis, Gait ataxia, Basal ganglia gliosis, Ataxia, Atrophy/Degeneration involving the caud... |
ORPHA:225154 |
| Obesity Due To Leptin Receptor Gene Deficiency |
|
Orthostatic hypotension due to autonomic dysfunction, Polyphagia, Emotional lability |
ORPHA:179494 |
| Schaaf-Yang Syndrome |
|
Skin-picking, Polyphagia, Impulsivity |
OMIM:615547 |
| Developmental Delay, Language Impairment, And Ocular Abnormalities |
|
Frequent temper tantrums, Aggressive behavior, Attention deficit hyperactivity disorder, Hyperact... |
OMIM:620141 |
| Hypotonia-Cystinuria Syndrome |
|
Polyphagia, Facial palsy |
OMIM:606407 |
| Temple Syndrome |
|
Polyphagia |
ORPHA:254516 |
| Bardet-Biedl Syndrome 9 |
|
Polyphagia, Polydipsia |
OMIM:615986 |
| Cebalid Syndrome |
|
Polyphagia |
OMIM:618774 |
| Histidinemia |
|
Hyperactivity |
ORPHA:2157 |
| Angelman Syndrome |
|
Self-injurious behavior, Optic atrophy, Inappropriate laughter, Recurrent hand flapping, Polyphag... |
ORPHA:72 |
| Frontotemporal Lobar Degeneration With Tdp43 Inclusions, Grn-Related |
|
Disinhibition, Polyphagia, Repetitive compulsive behavior, Agitation, Hypersexuality |
OMIM:607485 |
| Body Mass Index Quantitative Trait Locus 19 |
|
Polyphagia |
OMIM:617885 |
| Obesity Due To Congenital Leptin Deficiency |
|
Orthostatic hypotension due to autonomic dysfunction, Polyphagia |
ORPHA:66628 |
| Intellectual Developmental Disorder, X-Linked 107 |
|
Aggressive behavior, Attention deficit hyperactivity disorder, Hyperactivity |
OMIM:301013 |
| Man1B1-Cdg |
|
Polyphagia |
ORPHA:397941 |
| Insulinoma |
|
Polyphagia, Palpitations |
ORPHA:97279 |
| Intellectual Developmental Disorder, Autosomal Dominant 1 |
|
Self-injurious behavior, Bruxism, Inappropriate laughter, Recurrent hand flapping, Polyphagia, Ag... |
OMIM:156200 |
| Luscan-Lumish Syndrome |
|
Polyphagia, Aggressive behavior |
OMIM:616831 |
| Paternal Uniparental Disomy Of Chromosome 1 |
|
Polyphagia, Hypertension |
ORPHA:251004 |
| X-Linked Intellectual Disability-Acromegaly-Hyperactivity Syndrome |
|
Aggressive behavior, Hyperactivity |
ORPHA:85327 |
| Secondary Short Bowel Syndrome |
|
Aganglionic megacolon, Polyphagia |
ORPHA:95427 |
| Satb2-Associated Syndrome Due To A Chromosomal Rearrangement |
|
Emotional lability, Self-mutilation, Polyphagia, Aggressive behavior, Restlessness |
ORPHA:251028 |
| 7Q11.23 Microduplication Syndrome |
|
Self-injurious behavior, Aortic valve stenosis, Aggressive behavior, Polyphagia, Abnormal optic d... |
ORPHA:96121 |
| Obesity, Early-Onset, With Adrenal Insufficiency And Red Hair |
|
Polyphagia |
OMIM:609734 |
| Prader-Willi Syndrome Due To Paternal 15Q11Q13 Deletion |
|
Self-injurious behavior, Abnormal temper tantrums, Bulimia, Obsessive-compulsive trait, Polyphagi... |
ORPHA:98793 |
| Prader-Willi Syndrome Due To Paternal Deletion Of 15Q11Q13 Type 2 |
|
Self-injurious behavior, Abnormal temper tantrums, Bulimia, Obsessive-compulsive trait, Polyphagi... |
ORPHA:177904 |
| Prader-Willi Syndrome Due To Paternal Deletion Of 15Q11Q13 Type 1 |
|
Self-injurious behavior, Abnormal temper tantrums, Bulimia, Obsessive-compulsive trait, Polyphagi... |
ORPHA:177901 |
| Chromosome Xq26.3 Duplication Syndrome |
|
Polyphagia |
OMIM:300942 |
| Magel2-Related Prader-Willi-Like Syndrome |
|
Abnormal temper tantrums, Polyphagia, Skin-picking, Compulsive behaviors, Impulsivity |
ORPHA:398069 |
| Weaver Syndrome |
|
Polyphagia, Patent ductus arteriosus |
OMIM:277590 |
| Craniopharyngioma |
|
Optic atrophy, Cerebral ischemia, Polyphagia, Papilledema, Myocardial infarction |
ORPHA:54595 |
| Prader-Willi Syndrome Due To Maternal Uniparental Disomy Of Chromosome 15 |
|
Self-injurious behavior, Abnormal temper tantrums, Bulimia, Polyphagia, Skin-picking |
ORPHA:98754 |
| Sim1-Related Prader-Willi-Like Syndrome |
|
Abnormal temper tantrums, Polyphagia, Skin-picking |
ORPHA:398079 |
| Helsmoortel-Van Der Aa Syndrome |
|
Bruxism, Mitral regurgitation, Irritability, Polyphagia, Attention deficit hyperactivity disorder... |
OMIM:615873 |
| Prader-Willi Syndrome |
|
Polyphagia, Attention deficit hyperactivity disorder, Hypertension |
ORPHA:739 |
| Gangliocytoma |
|
Polyphagia |
ORPHA:251937 |
| Porphyria Due To Ala Dehydratase Deficiency |
|
Depression, Restlessness, Abnormal fear-induced behavior, Agitation |
ORPHA:100924 |
| Supranuclear Palsy, Progressive, 1 |
|
Memory impairment, Cerebral atrophy, Frontolimbic dementia, Astrocytosis, Gliosis, Neuronal loss ... |
OMIM:601104 |
| Adnp Syndrome |
|
Abnormal temper tantrums, Oral-pharyngeal dysphagia, Polyphagia, Attention deficit hyperactivity ... |
ORPHA:404448 |
| Pseudohypoparathyroidism Type 1A |
|
Depression, Irritability, Polyphagia, Prolonged QT interval, Hypertension |
ORPHA:79443 |
| Prader-Willi Syndrome |
|
Self-injurious behavior, Polyphagia, Attention deficit hyperactivity disorder |
OMIM:176270 |
| Pseudohypoparathyroidism Type 1C |
|
Prolonged QT interval, Polyphagia, Depression, Irritability |
ORPHA:79444 |
| Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome |
|
Self-injurious behavior, Depression, Polydipsia, Emotional lability, Polyphagia, Aggressive behav... |
ORPHA:293987 |
| Intellectual Developmental Disorder, Autosomal Dominant 71, With Behavioral Abnormalities |
|
Self-injurious behavior, Fixated interests, Emotional lability, Hair-pulling, Polyphagia, Attenti... |
OMIM:620330 |
| Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy |
|
Astrocytosis |
OMIM:611087 |
| 1P36 Deletion Syndrome |
|
Self-injurious behavior, Optic atrophy, Dilated cardiomyopathy, Telangiectasia, Polyphagia, Motor... |
ORPHA:1606 |
| Gm2 Gangliosidosis, Ab Variant |
|
Abnormal fear-induced behavior, Inappropriate behavior |
ORPHA:309246 |
| Pituitary Adenoma 4, Acth-Secreting |
|
Abnormal fear-induced behavior, Hypertension, Emotional lability |
OMIM:219090 |
| Chromosome 1P36 Deletion Syndrome, Distal |
|
Optic atrophy, Dilated cardiomyopathy, Optic disc coloboma, Oppositional defiant disorder, Self-m... |
OMIM:607872 |
| Mitochondrial Dna Depletion Syndrome 4A (Alpers Type) |
|
Cerebellar atrophy, Cerebral atrophy, Cerebral cortical neurodegeneration, Astrocytosis, Gliosis,... |
OMIM:203700 |
| X-Linked Acrogigantism |
|
Polyphagia |
ORPHA:300373 |
| Lipodystrophy, Congenital Generalized, Type 1 |
|
Polyphagia, Cardiomyopathy |
OMIM:608594 |
| Lipodystrophy, Congenital Generalized, Type 2 |
|
Hypertrophic cardiomyopathy, Polyphagia |
OMIM:269700 |
| Rubinstein-Taybi Syndrome Due To 16P13.3 Microdeletion |
|
Self-injurious behavior, Aortic valve stenosis, Abnormal fear-induced behavior, Emotional labilit... |
ORPHA:353281 |
| Laminin Subunit Alpha 2-Related Congenital Muscular Dystrophy |
|
Astrocytosis, Cognitive impairment, Pontocerebellar atrophy |
ORPHA:258 |
| Cirrhosis-Dystonia-Polycythemia-Hypermanganesemia Syndrome |
|
Truncal ataxia, Astrocytosis, Dysdiadochokinesis |
ORPHA:309854 |
| Cockayne Syndrome Type 3 |
|
Progressive neurologic deterioration, Astrocytosis, Brain atrophy, Cognitive impairment |
ORPHA:90324 |
| Rubinstein-Taybi Syndrome Due To Ep300 Haploinsufficiency |
|
Self-injurious behavior, Aortic valve stenosis, Abnormal fear-induced behavior, Emotional labilit... |
ORPHA:353284 |
| Rubinstein-Taybi Syndrome Due To Crebbp Mutations |
|
Self-injurious behavior, Aortic valve stenosis, Abnormal fear-induced behavior, Emotional labilit... |
ORPHA:353277 |
| Alström Syndrome |
|
Dilated cardiomyopathy, Congestive heart failure, Portal hypertension, Polyphagia, Pulmonary arte... |
ORPHA:64 |
