Triglyceride Storage Disease, Type Ii |
|
Obesity |
OMIM:190430 |
Maturity-Onset Diabetes Of The Young, Type 11 |
|
Obesity, Overweight |
OMIM:613375 |
Obesity |
|
Obesity, Increased waist to hip ratio |
OMIM:601665 |
Spermatogenic Failure, X-Linked, 1 |
|
Obesity |
OMIM:305700 |
Abdominal Obesity-Metabolic Syndrome 1 |
|
Abdominal obesity |
OMIM:605552 |
Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 |
|
Abdominal obesity |
OMIM:605572 |
Prader-Willi Syndrome (Type 2) |
|
Truncal obesity |
DECIPHER:53 |
Prader-Willi syndrome (Type 1) |
|
Truncal obesity |
DECIPHER:14 |
Epidermodysplasia Verruciformis, Susceptibility To, 2 |
|
Verruca plana, Squamous cell carcinoma of the skin |
OMIM:618231 |
Bardet-Biedl Syndrome 11 |
|
Obesity |
OMIM:615988 |
Thumb Stiffness-Brachydactyly-Intellectual Disability Syndrome |
|
Obesity |
ORPHA:1078 |
Bardet-Biedl Syndrome 14 |
|
Obesity |
OMIM:615991 |
Adenocarcinoma Of The Esophagus |
|
Barrett esophagus, Obesity, Esophageal carcinoma |
ORPHA:99976 |
Bardet-Biedl Syndrome 13 |
|
Obesity |
OMIM:615990 |
Intellectual Developmental Disorder, X-Linked 97 |
|
Obesity |
OMIM:300803 |
Hypoinsulinemic Hypoglycemia And Body Hemihypertrophy |
|
Large for gestational age, Truncal obesity |
ORPHA:293964 |
Hyperinsulinemic Hypoglycemia, Familial, 1 |
|
Large for gestational age |
OMIM:256450 |
Pilomatrixoma |
|
Pilomatrixoma |
OMIM:132600 |
Hyperinsulinemic Hypoglycemia, Familial, 2 |
|
Large for gestational age |
OMIM:601820 |
Bardet-Biedl Syndrome 18 |
|
Obesity |
OMIM:615995 |
Hypoinsulinemic Hypoglycemia With Hemihypertrophy |
|
Large for gestational age, Obesity, Truncal obesity |
OMIM:240900 |
Adiposis Dolorosa |
|
Painful subcutaneous lipomas, Obesity |
OMIM:103200 |
Body Mass Index Quantitative Trait Locus 20 |
|
Tall stature, Obesity |
OMIM:618406 |
Mitochondrial Complex Iv Deficiency, Nuclear Type 14 |
|
Obesity |
OMIM:619058 |
Autism, Susceptibility To, X-Linked 6 |
|
Obesity |
OMIM:300872 |
Bardet-Biedl Syndrome 10 |
|
Obesity |
OMIM:615987 |
Cutaneous Neuroendocrine Carcinoma |
|
Neoplasm of the outer ear, Squamous cell carcinoma of the skin, Merkel cell skin cancer, Carcinoi... |
ORPHA:79140 |
Familial Multinodular Goiter |
|
Sertoli cell neoplasm, Pleuropulmonary blastoma, Alveolar rhabdomyosarcoma, Thyroid carcinoma, Pi... |
ORPHA:276399 |
Coronary Artery Disease, Autosomal Dominant, 1 |
|
Obesity |
OMIM:608320 |
Obesity And Hypopigmentation |
|
Overgrowth, Obesity |
OMIM:620195 |
Ankylosing Vertebral Hyperostosis With Tylosis |
|
Obesity |
ORPHA:2206 |
Palmoplantar Keratoderma-Xx Sex Reversal-Predisposition To Squamous Cell Carcinoma Syndrome |
|
Squamous cell carcinoma of the skin |
ORPHA:85112 |
Prolactin Deficiency With Obesity And Enlarged Testes |
|
Obesity |
OMIM:264120 |
Apc-Related Attenuated Familial Adenomatous Polyposis |
|
Osteoma, Fibrosarcoma, Desmoid tumors, Adrenocortical adenoma, Medulloblastoma, Multiple gastric ... |
ORPHA:247806 |
Epidermodysplasia Verruciformis, Susceptibility To, 5 |
|
Squamous cell carcinoma of the skin, Verrucae |
OMIM:618309 |
Microduplication Xp11.22P11.23 Syndrome |
|
Obesity |
ORPHA:217377 |
Obesity Due To Melanocortin 4 Receptor Deficiency |
|
Obesity, Childhood-onset truncal obesity |
ORPHA:71529 |
Severe Early-Onset Obesity-Insulin Resistance Syndrome Due To Sh2B1 Deficiency |
|
Obesity |
ORPHA:329249 |
Bardet-Biedl Syndrome 22 |
|
Obesity, Large for gestational age |
OMIM:617119 |
Pilomatrixoma |
|
Neoplasm of head and neck, Pilomatrixoma |
ORPHA:91414 |
Gardner Syndrome |
|
Colon cancer, Ampulla of Vater carcinoma, Hepatoblastoma, Brain neoplasm, Osteoma, Fibrosarcoma, ... |
ORPHA:79665 |
Obesity-Colitis-Hypothyroidism-Cardiac Hypertrophy-Developmental Delay Syndrome |
|
Obesity |
ORPHA:88643 |
Obesity-Hypoventilation Syndrome |
|
Obesity |
OMIM:257500 |
Cortisone Reductase Deficiency 2 |
|
Obesity |
OMIM:614662 |
Polycystic Ovary Syndrome 1 |
|
Obesity |
OMIM:184700 |
Hypothyroidism, Central, With Testicular Enlargement |
|
Overweight |
OMIM:300888 |
Cortisone Reductase Deficiency 1 |
|
Obesity |
OMIM:604931 |
Hepatic Veno-Occlusive Disease |
|
Increased body weight |
ORPHA:890 |
Obesity, Hyperphagia, And Developmental Delay |
|
Obesity |
OMIM:613886 |
Coenzyme Q10 Deficiency, Primary, 2 |
|
Obesity, Overweight |
OMIM:614651 |
Bardet-Biedl Syndrome 8 |
|
Obesity |
OMIM:615985 |
Huriez Syndrome |
|
Squamous cell carcinoma of the skin |
OMIM:181600 |
Hypothyroidism, Congenital, Nongoitrous, 6 |
|
Increased body weight, Increased body mass index |
OMIM:614450 |
Hypogonadotropic Hypogonadism 27 Without Anosmia |
|
Obesity |
OMIM:619755 |
Turcot Syndrome With Polyposis |
|
Glioma, Hepatoblastoma, Brain neoplasm, Desmoid tumors, Leukemia, Basal cell carcinoma, Glioblast... |
ORPHA:99818 |
Phip-Related Behavioral Problems-Intellectual Disability-Obesity-Dysmorphic Features Syndrome |
|
Increased body weight |
ORPHA:589905 |
Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome |
|
Increased body weight |
ORPHA:276608 |
Mosaic Variegated Aneuploidy Syndrome 7 With Inflammation And Tumor Predisposition |
|
Pilomatrixoma, Embryonal rhabdomyosarcoma, Cervix cancer, Adenocarcinoma of the colon, Lipoma, Mu... |
OMIM:620189 |
Disabling Pansclerotic Morphea Of Childhood |
|
Squamous cell carcinoma of the skin |
OMIM:620443 |
Xeroderma Pigmentosum, Complementation Group E |
|
Basal cell carcinoma, Squamous cell carcinoma of the skin, Melanoma |
OMIM:278740 |
Acth-Independent Macronodular Adrenal Hyperplasia 2 |
|
Increased body weight, Abdominal obesity |
OMIM:615954 |
Thyroid Hormone Resistance, Generalized, Autosomal Recessive |
|
Increased body weight, Small for gestational age |
OMIM:274300 |
Xeroderma Pigmentosum, Complementation Group C |
|
Basal cell carcinoma, Squamous cell carcinoma of the skin, Actinic keratosis, Cutaneous melanoma |
OMIM:278720 |
Wilms Tumor, Aniridia, Genitourinary Anomalies, And Impaired Intellectual Development Syndrome |
|
Gonadoblastoma, Obesity, Nephroblastoma |
OMIM:194072 |
Pseudohypoparathyroidism, Type Ib |
|
Obesity |
OMIM:603233 |
Insulinoma |
|
Neuroendocrine neoplasm, Pituitary prolactin cell adenoma, Zollinger-Ellison syndrome, Increased ... |
ORPHA:97279 |
Blue Diaper Syndrome |
|
Increased body weight |
ORPHA:94086 |
Oculocutaneous Albinism Type 1B |
|
Basal cell carcinoma, Squamous cell carcinoma of the skin, Melanoma |
ORPHA:79434 |
Dyskeratosis Congenita, Digenic |
|
Basal cell carcinoma, Melanoma, Squamous cell carcinoma of the skin, Failure to thrive |
OMIM:620040 |
Pulmonary Fibrosis And/Or Bone Marrow Failure Syndrome, Telomere-Related, 7 |
|
Squamous cell carcinoma of the skin, Myelodysplasia |
OMIM:620365 |
Xeroderma Pigmentosum, Complementation Group B |
|
Basal cell carcinoma, Squamous cell carcinoma of the skin, Neoplasm, Cutaneous melanoma |
OMIM:610651 |
Xeroderma Pigmentosum-Cockayne Syndrome Complex |
|
Basal cell carcinoma, Melanoma, Cachexia, Squamous cell carcinoma of the skin |
ORPHA:220295 |
Intellectual Developmental Disorder, X-Linked, Syndromic, Nascimento Type |
|
Increased body weight |
OMIM:300860 |
Smith-Magenis Syndrome |
|
Increased body weight |
OMIM:182290 |
Oculocutaneous Albinism Type 1A |
|
Basal cell carcinoma, Squamous cell carcinoma of the skin |
ORPHA:79431 |
Narcolepsy 7 |
|
Obesity |
OMIM:614250 |
Wilson Disease |
|
Increased body weight, Weight loss, Failure to thrive |
ORPHA:905 |
Adrenocortical Carcinoma |
|
Increased body weight, Weight loss, Adrenocortical carcinoma, Lung adenocarcinoma |
ORPHA:1501 |
Congenital Hyperinsulinism Due To Hnf4A Deficiency |
|
Increased body weight, Large for gestational age |
ORPHA:263455 |
Pruritic Urticarial Papules And Plaques Of Pregnancy |
|
Increased body weight |
ORPHA:64745 |
Carney Complex |
|
Follicular thyroid carcinoma, Tall stature, Increased body weight, Neoplasm of the pharynx, Ovari... |
ORPHA:1359 |
Low Phospholipid-Associated Cholelithiasis |
|
Obesity, Overweight, Neoplasm of the liver, Hepatocellular carcinoma |
ORPHA:69663 |
Pigmented Nodular Adrenocortical Disease, Primary, 4 |
|
Increased body weight |
OMIM:615830 |
Xeroderma Pigmentosum, Complementation Group A |
|
Melanoma, Squamous cell carcinoma of the skin |
OMIM:278700 |
Cushing Syndrome Due To Bilateral Macronodular Adrenocortical Disease |
|
Pituitary adenoma, Neuroendocrine neoplasm, Meningioma, Increased body weight, Renal cell carcino... |
ORPHA:189427 |
Sotos Syndrome |
|
Increased body weight, Tall stature, Overgrowth |
OMIM:117550 |
Oculocutaneous Albinism Type 2 |
|
Basal cell carcinoma, Squamous cell carcinoma of the skin, Cutaneous melanoma |
ORPHA:79432 |
Hermansky-Pudlak Syndrome |
|
Basal cell carcinoma, Squamous cell carcinoma of the skin, Weight loss |
ORPHA:79430 |
Glycogen Storage Disease Due To Liver And Muscle Phosphorylase Kinase Deficiency |
|
Increased body weight, Hepatocellular adenoma, Hepatocellular carcinoma |
ORPHA:79240 |
Glycogen Storage Disease Due To Liver Phosphorylase Kinase Deficiency |
|
Increased body weight, Hepatocellular adenoma, Failure to thrive |
ORPHA:264580 |
Insulin-Resistance Syndrome Type B |
|
Lymphoma, Abnormality of body weight, Decreased body weight, Increased body weight, Hodgkin lymph... |
ORPHA:2298 |
Autosomal Dominant Generalized Epidermolysis Bullosa Simplex, Severe Form |
|
Squamous cell carcinoma of the skin, Failure to thrive |
ORPHA:79396 |
Lmna-Related Cardiocutaneous Progeria Syndrome |
|
Basal cell carcinoma, Squamous cell carcinoma of the skin, Papillary renal cell carcinoma, Pulmon... |
ORPHA:363618 |
Dyskeratosis Congenita, Autosomal Dominant 1 |
|
Squamous cell carcinoma of the skin, Myelodysplasia |
OMIM:127550 |
Magel2-Related Prader-Willi-Like Syndrome |
|
Increased body weight, Failure to thrive, Abdominal obesity |
ORPHA:398069 |
Cushing Syndrome Due To Ectopic Acth Secretion |
|
Small cell lung carcinoma, Malignant gastrointestinal tract tumors, Pulmonary carcinoid tumor, Ne... |
ORPHA:99889 |
Rubinstein-Taybi Syndrome Due To 16P13.3 Microdeletion |
|
Failure to thrive, Meningioma, Obesity, Neoplasm, Pilomatrixoma, Spinal cord tumor |
ORPHA:353281 |
Hellp Syndrome |
|
Increased body weight |
ORPHA:244242 |
Cushing Disease |
|
Increased body weight, Pituitary corticotropic cell adenoma, Truncal obesity, Abdominal obesity |
ORPHA:96253 |
Rubinstein-Taybi Syndrome Due To Ep300 Haploinsufficiency |
|
Obesity, Failure to thrive, Pilomatrixoma, Meningioma |
ORPHA:353284 |
Rubinstein-Taybi Syndrome Due To Crebbp Mutations |
|
Obesity, Failure to thrive, Pilomatrixoma, Meningioma |
ORPHA:353277 |
Tetrasomy 9P |
|
Pilomatrixoma |
ORPHA:3310 |