Obesity Due To Melanocortin 4 Receptor Deficiency |
|
Increased adipose tissue, Obesity, Childhood-onset truncal obesity, Polyphagia |
ORPHA:71529 |
Macrosomia Adiposa Congenita |
|
Obesity, Polyphagia, Large for gestational age |
OMIM:248100 |
Kleine-Levin Hibernation Syndrome |
|
Polyphagia |
OMIM:148840 |
Body Mass Index Quantitative Trait Locus 20 |
|
Obesity, Polyphagia |
OMIM:618406 |
Obesity Due To Prohormone Convertase I Deficiency |
|
Increased adipose tissue, Polyphagia, Failure to thrive, Obesity, Childhood-onset truncal obesity |
ORPHA:71528 |
Obesity Due To Pro-Opiomelanocortin Deficiency |
|
Increased adipose tissue, Polyphagia, Failure to thrive, Obesity, Childhood-onset truncal obesity |
ORPHA:71526 |
Obesity, Hyperphagia, And Developmental Delay |
|
Obesity, Polyphagia |
OMIM:613886 |
Severe Early-Onset Obesity-Insulin Resistance Syndrome Due To Sh2B1 Deficiency |
|
Obesity, Polyphagia |
ORPHA:329249 |
Leptin Deficiency Or Dysfunction |
|
Obesity, Abnormal eating behavior, Polyphagia |
OMIM:614962 |
Bardet-Biedl Syndrome 22 |
|
Obesity, Polyphagia, Large for gestational age |
OMIM:617119 |
Renal Glucosuria |
|
Polyphagia, Polydipsia |
OMIM:233100 |
Hypotonia-Cystinuria Syndrome |
|
Failure to thrive, Polyphagia |
ORPHA:163690 |
Obesity Due To Sim1 Deficiency |
|
Obesity, Polyphagia |
ORPHA:369873 |
Obesity, Early-Onset, With Adrenal Insufficiency And Red Hair |
|
Obesity, Polyphagia |
OMIM:609734 |
Type 1 Diabetes Mellitus |
|
Polyphagia, Polydipsia |
OMIM:222100 |
Leptin Receptor Deficiency |
|
Obesity, Abnormal eating behavior, Polyphagia |
OMIM:614963 |
Prader-Willi Syndrome Due To Imprinting Mutation |
|
Obesity, Polyphagia |
ORPHA:177910 |
Pick Disease Of Brain |
|
Polyphagia |
OMIM:172700 |
Graves Disease, Susceptibility To, 1 |
|
Weight loss, Polyphagia |
OMIM:275000 |
Frontotemporal Dementia |
|
Polyphagia |
OMIM:600274 |
Angelman Syndrome Due To Imprinting Defect In 15Q11-Q13 |
|
Obesity, Polyphagia |
ORPHA:411515 |
Bardet-Biedl Syndrome 9 |
|
Obesity, Polydipsia, Truncal obesity, Polyphagia |
OMIM:615986 |
6Q16 Microdeletion Syndrome |
|
Obesity, Polyphagia |
ORPHA:171829 |
Schaaf-Yang Syndrome |
|
Failure to thrive in infancy, Polyphagia, Arthrogryposis multiplex congenita, Flexion contracture... |
OMIM:615547 |
Temple Syndrome |
|
Obesity, Small for gestational age, Polyphagia |
ORPHA:254516 |
Hyperinsulinism Due To Hnf1A Deficiency |
|
Small for gestational age, Polyphagia, Large for gestational age |
ORPHA:324575 |
Hyperinsulinism Due To Ucp2 Deficiency |
|
Polyphagia, Large for gestational age |
ORPHA:276556 |
Huntington Disease |
|
Polyphagia, Decreased body mass index, Choking episodes, Weight loss, Oral-pharyngeal dysphagia |
ORPHA:399 |
Cebalid Syndrome |
|
Congenital diaphragmatic hernia, Polyphagia |
OMIM:618774 |
Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency |
|
Polyphagia, Large for gestational age |
ORPHA:276575 |
Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency |
|
Polyphagia, Large for gestational age |
ORPHA:276580 |
Hypotonia-Cystinuria Syndrome |
|
Failure to thrive, Polyphagia |
OMIM:606407 |
Man1B1-Cdg |
|
Truncal obesity, Polyphagia |
ORPHA:397941 |
Chromosome 22Q13 Duplication Syndrome |
|
Polyphagia |
OMIM:615538 |
Insulinoma |
|
Increased body weight, Polyphagia |
ORPHA:97279 |
2Q23.1 Microdeletion Syndrome |
|
Polyphagia |
ORPHA:228402 |
Trisomy 18P |
|
Polyphagia |
ORPHA:1715 |
Obesity Due To Congenital Leptin Deficiency |
|
Obesity, Polyphagia |
ORPHA:66628 |
Luscan-Lumish Syndrome |
|
Obesity, Polyphagia |
OMIM:616831 |
Paternal Uniparental Disomy Of Chromosome 1 |
|
Obesity, Abnormal dental enamel morphology, Polyphagia |
ORPHA:251004 |
Obesity Due To Leptin Receptor Gene Deficiency |
|
Obesity, Polyphagia |
ORPHA:179494 |
Secondary Short Bowel Syndrome |
|
Failure to thrive, Weight loss, Polyphagia |
ORPHA:95427 |
Pediatric-Onset Graves Disease |
|
Failure to thrive, Polydipsia, Polyphagia |
ORPHA:525731 |
Intellectual Developmental Disorder, Autosomal Dominant 1 |
|
Polyphagia |
OMIM:156200 |
Lipodystrophy, Congenital Generalized, Type 1 |
|
Polyphagia, Reduced intrathoracic adipose tissue, Lipodystrophy, Reduced subcutaneous adipose tis... |
OMIM:608594 |
Chromosome Xq26.3 Duplication Syndrome |
|
Polyphagia |
OMIM:300942 |
Lipodystrophy, Congenital Generalized, Type 2 |
|
Polyphagia, Reduced intrathoracic adipose tissue, Lipodystrophy, Reduced subcutaneous adipose tis... |
OMIM:269700 |
Magel2-Related Prader-Willi-Like Syndrome |
|
Polyphagia, Failure to thrive, Abdominal obesity, Flexion contracture, Increased body weight |
ORPHA:398069 |
Sim1-Related Prader-Willi-Like Syndrome |
|
Failure to thrive, Obesity, Abdominal obesity, Polyphagia |
ORPHA:398079 |
Angelman Syndrome |
|
Obesity, Dysphagia, Polyphagia |
ORPHA:72 |
Prader-Willi Syndrome Due To Maternal Uniparental Disomy Of Chromosome 15 |
|
Small for gestational age, Polyphagia, Failure to thrive, Bulimia, Obesity |
ORPHA:98754 |
Prader-Willi Syndrome Due To Paternal 15Q11Q13 Deletion |
|
Small for gestational age, Polyphagia, Failure to thrive, Bulimia, Obesity |
ORPHA:98793 |
Prader-Willi Syndrome Due To Paternal Deletion Of 15Q11Q13 Type 2 |
|
Small for gestational age, Polyphagia, Failure to thrive, Bulimia, Obesity |
ORPHA:177904 |
Prader-Willi Syndrome Due To Paternal Deletion Of 15Q11Q13 Type 1 |
|
Small for gestational age, Polyphagia, Failure to thrive, Bulimia, Obesity |
ORPHA:177901 |
Prader-Willi Syndrome |
|
Obesity, Failure to thrive in infancy, Abdominal obesity, Polyphagia |
OMIM:176270 |
Frontotemporal Lobar Degeneration With Tdp43 Inclusions, Grn-Related |
|
Polyphagia |
OMIM:607485 |
Satb2-Associated Syndrome Due To A Chromosomal Rearrangement |
|
Polyphagia |
ORPHA:251028 |
Gangliocytoma |
|
Polyphagia |
ORPHA:251937 |
7Q11.23 Microduplication Syndrome |
|
Congenital diaphragmatic hernia, Obesity, Inguinal hernia, Polyphagia |
ORPHA:96121 |
Prader-Willi-Like Syndrome |
|
Small for gestational age, Polyphagia, Failure to thrive, Bulimia, Obesity |
ORPHA:398073 |
X-Linked Acrogigantism |
|
Increased body mass index, Polyphagia |
ORPHA:300373 |
Adnp Syndrome |
|
Polyphagia, Inguinal hernia, Truncal obesity, Oral-pharyngeal dysphagia, Umbilical hernia |
ORPHA:404448 |
Prader-Willi Syndrome |
|
Failure to thrive, Abdominal obesity, Polyphagia |
ORPHA:739 |
Pseudohypoparathyroidism Type 1C |
|
Obesity, Enamel hypoplasia, Polyphagia |
ORPHA:79444 |
Craniopharyngioma |
|
Obesity, Polyphagia |
ORPHA:54595 |
Pseudohypoparathyroidism Type 1A |
|
Obesity, Enamel hypoplasia, Polyphagia |
ORPHA:79443 |
1P36 Deletion Syndrome |
|
Dysphagia, Polyphagia, Failure to thrive, Camptodactyly of finger, Obesity |
ORPHA:1606 |
Early-Onset Schizophrenia |
|
Polyphagia |
ORPHA:96369 |
Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome |
|
Obesity, Polydipsia, Polyphagia |
ORPHA:293987 |
Chromosome 1P36 Deletion Syndrome, Distal |
|
Dysphagia, Polyphagia, Camptodactyly of finger, Camptodactyly, Obesity |
OMIM:607872 |
Obesity |
|
Obesity, Increased waist to hip ratio |
OMIM:601665 |
Alström Syndrome |
|
Obesity, Dorsocervical fat pad, Truncal obesity, Polyphagia |
ORPHA:64 |