Obesity Due To Melanocortin 4 Receptor Deficiency |
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Childhood-onset truncal obesity, Obesity, Increased adipose tissue, Polyphagia |
ORPHA:71529 |
Macrosomia Adiposa Congenita |
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Obesity, Polyphagia, Large for gestational age |
OMIM:248100 |
Kleine-Levin Hibernation Syndrome |
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Polyphagia |
OMIM:148840 |
Body Mass Index Quantitative Trait Locus 20 |
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Obesity, Polyphagia |
OMIM:618406 |
Obesity Due To Prohormone Convertase I Deficiency |
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Childhood-onset truncal obesity, Increased adipose tissue, Failure to thrive, Polyphagia, Obesity |
ORPHA:71528 |
Obesity Due To Pro-Opiomelanocortin Deficiency |
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Childhood-onset truncal obesity, Increased adipose tissue, Failure to thrive, Polyphagia, Obesity |
ORPHA:71526 |
Obesity, Hyperphagia, And Developmental Delay |
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Obesity, Polyphagia |
OMIM:613886 |
Bardet-Biedl Syndrome 22 |
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Obesity, Polyphagia, Large for gestational age |
OMIM:617119 |
Hypermetabolism Due To Uncoupled Mitochondrial Oxidative Phosphorylation 2 |
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Failure to thrive, Polyphagia, Decreased body weight |
OMIM:620085 |
Leptin Deficiency Or Dysfunction |
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Obesity, Polyphagia |
OMIM:614962 |
Severe Early-Onset Obesity-Insulin Resistance Syndrome Due To Sh2B1 Deficiency |
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Obesity, Polyphagia |
ORPHA:329249 |
Renal Glucosuria |
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Polyphagia, Polydipsia |
OMIM:233100 |
Hypotonia-Cystinuria Syndrome |
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Failure to thrive, Polyphagia |
ORPHA:163690 |
Type 1 Diabetes Mellitus |
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Polyphagia, Polydipsia |
OMIM:222100 |
Obesity Due To Sim1 Deficiency |
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Attention deficit hyperactivity disorder, Polyphagia, Obesity |
ORPHA:369873 |
Pick Disease Of Brain |
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Disinhibition, Polyphagia |
OMIM:172700 |
Prader-Willi Syndrome Due To Imprinting Mutation |
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Obesity, Polyphagia |
ORPHA:177910 |
Leptin Receptor Deficiency |
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Obesity, Polyphagia, Abnormal eating behavior |
OMIM:614963 |
Intellectual Developmental Disorder, Autosomal Dominant 39 |
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Obesity, Polyphagia |
OMIM:616521 |
Frontotemporal Dementia |
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Disinhibition, Polyphagia |
OMIM:600274 |
Angelman Syndrome Due To Imprinting Defect In 15Q11-Q13 |
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Hyperactivity, Obesity, Polyphagia |
ORPHA:411515 |
Graves Disease, Susceptibility To, 1 |
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Hyperactivity, Polyphagia, Weight loss |
OMIM:275000 |
Body Mass Index Quantitative Trait Locus 19 |
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Obesity, Polyphagia |
OMIM:617885 |
Huntington Disease |
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Weight loss, Choking episodes, Agitation, Polyphagia, Decreased body mass index, Disinhibition, A... |
ORPHA:399 |
Hyperinsulinism Due To Hnf1A Deficiency |
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Small for gestational age, Polyphagia, Large for gestational age, Agitation |
ORPHA:324575 |
Hyperinsulinism Due To Ucp2 Deficiency |
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Polyphagia, Large for gestational age, Agitation |
ORPHA:276556 |
Schaaf-Yang Syndrome |
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Flexion contracture, Camptodactyly, Impulsivity, Polyphagia, Obesity, Failure to thrive in infanc... |
OMIM:615547 |
Bardet-Biedl Syndrome 9 |
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Obesity, Polyphagia, Polydipsia, Truncal obesity |
OMIM:615986 |
6Q16 Microdeletion Syndrome |
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Obesity, Polyphagia |
ORPHA:171829 |
Temple Syndrome |
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Small for gestational age, Obesity, Polyphagia |
ORPHA:254516 |
Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency |
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Polyphagia, Large for gestational age, Agitation |
ORPHA:276575 |
Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency |
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Polyphagia, Large for gestational age, Agitation |
ORPHA:276580 |
Cebalid Syndrome |
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Congenital diaphragmatic hernia, Polyphagia |
OMIM:618774 |
Chromosome 22Q13 Duplication Syndrome |
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Impulsivity, Attention deficit hyperactivity disorder, Polyphagia |
OMIM:615538 |
Hypotonia-Cystinuria Syndrome |
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Failure to thrive, Polyphagia |
OMIM:606407 |
2Q23.1 Microdeletion Syndrome |
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Hyperactivity, Polyphagia |
ORPHA:228402 |
Man1B1-Cdg |
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Polyphagia, Truncal obesity |
ORPHA:397941 |
Obesity, Early-Onset, With Adrenal Insufficiency And Red Hair |
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Obesity, Polyphagia |
OMIM:609734 |
Trisomy 18P |
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Attention deficit hyperactivity disorder, Polyphagia |
ORPHA:1715 |
Insulinoma |
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Polyphagia, Increased body weight |
ORPHA:97279 |
Obesity Due To Congenital Leptin Deficiency |
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Obesity, Polyphagia |
ORPHA:66628 |
Pediatric-Onset Graves Disease |
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Failure to thrive, Hyperactivity, Polyphagia, Polydipsia |
ORPHA:525731 |
Obesity Due To Leptin Receptor Gene Deficiency |
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Obesity, Polyphagia |
ORPHA:179494 |
Secondary Short Bowel Syndrome |
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Failure to thrive, Polyphagia, Weight loss |
ORPHA:95427 |
Luscan-Lumish Syndrome |
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Obesity, Polyphagia |
OMIM:616831 |
Paternal Uniparental Disomy Of Chromosome 1 |
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Obesity, Polyphagia, Abnormal dental enamel morphology |
ORPHA:251004 |
Frontotemporal Lobar Degeneration With Tdp43 Inclusions, Grn-Related |
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Disinhibition, Polyphagia, Agitation |
OMIM:607485 |
Wagro Syndrome |
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Obesity, Polyphagia, Agitation |
OMIM:612469 |
Magel2-Related Prader-Willi-Like Syndrome |
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Flexion contracture, Failure to thrive, Impulsivity, Polyphagia, Abdominal obesity, Increased bod... |
ORPHA:398069 |
Angelman Syndrome |
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Hyperactivity, Obesity, Polyphagia, Dysphagia |
ORPHA:72 |
Lipodystrophy, Congenital Generalized, Type 1 |
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Reduced intraabdominal adipose tissue, Reduced subcutaneous adipose tissue, Lipodystrophy, Reduce... |
OMIM:608594 |
Chromosome Xq26.3 Duplication Syndrome |
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Polyphagia |
OMIM:300942 |
Sim1-Related Prader-Willi-Like Syndrome |
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Failure to thrive, Obesity, Polyphagia, Abdominal obesity |
ORPHA:398079 |
Prader-Willi Syndrome Due To Maternal Uniparental Disomy Of Chromosome 15 |
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Small for gestational age, Bulimia, Failure to thrive, Polyphagia, Obesity |
ORPHA:98754 |
Lipodystrophy, Congenital Generalized, Type 2 |
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Reduced intraabdominal adipose tissue, Reduced subcutaneous adipose tissue, Lipodystrophy, Reduce... |
OMIM:269700 |
Weaver Syndrome |
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Joint contracture of the hand, Camptodactyly, Inguinal hernia, Polyphagia, Umbilical hernia |
OMIM:277590 |
Satb2-Associated Syndrome Due To A Chromosomal Rearrangement |
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Restlessness, Polyphagia |
ORPHA:251028 |
Prader-Willi Syndrome Due To Paternal 15Q11Q13 Deletion |
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Small for gestational age, Bulimia, Failure to thrive, Polyphagia, Obesity |
ORPHA:98793 |
Prader-Willi Syndrome Due To Paternal Deletion Of 15Q11Q13 Type 2 |
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Small for gestational age, Bulimia, Failure to thrive, Polyphagia, Obesity |
ORPHA:177904 |
Intellectual Developmental Disorder, Autosomal Dominant 1 |
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Polyphagia |
OMIM:156200 |
Prader-Willi Syndrome Due To Paternal Deletion Of 15Q11Q13 Type 1 |
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Small for gestational age, Bulimia, Failure to thrive, Polyphagia, Obesity |
ORPHA:177901 |
7Q11.23 Microduplication Syndrome |
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Hyperactivity, Inguinal hernia, Congenital diaphragmatic hernia, Polyphagia, Obesity |
ORPHA:96121 |
Prader-Willi-Like Syndrome |
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Small for gestational age, Bulimia, Failure to thrive, Polyphagia, Obesity |
ORPHA:398073 |
Prader-Willi Syndrome |
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Attention deficit hyperactivity disorder, Polyphagia, Obesity, Failure to thrive in infancy, Abdo... |
OMIM:176270 |
Gangliocytoma |
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Polyphagia |
ORPHA:251937 |
Adnp Syndrome |
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Inguinal hernia, Attention deficit hyperactivity disorder, Polyphagia, Truncal obesity, Umbilical... |
ORPHA:404448 |
Prader-Willi Syndrome |
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Failure to thrive, Attention deficit hyperactivity disorder, Polyphagia, Abdominal obesity |
ORPHA:739 |
Early-Onset Schizophrenia |
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Addictive behavior, Restlessness, Attention deficit hyperactivity disorder, Polyphagia |
ORPHA:96369 |
X-Linked Acrogigantism |
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Polyphagia, Increased body mass index |
ORPHA:300373 |
Pseudohypoparathyroidism Type 1C |
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Enamel hypoplasia, Obesity, Polyphagia |
ORPHA:79444 |
Helsmoortel-Van Der Aa Syndrome |
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Hyperactivity, Failure to thrive, Truncal obesity, Polyphagia, Attention deficit hyperactivity di... |
OMIM:615873 |
Pseudohypoparathyroidism Type 1A |
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Enamel hypoplasia, Obesity, Polyphagia |
ORPHA:79443 |
Craniopharyngioma |
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Obesity, Polyphagia |
ORPHA:54595 |
1P36 Deletion Syndrome |
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Camptodactyly of finger, Failure to thrive, Polyphagia, Dysphagia, Obesity |
ORPHA:1606 |
Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome |
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Obesity, Polyphagia, Polydipsia |
ORPHA:293987 |
Chromosome 1P36 Deletion Syndrome, Distal |
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Camptodactyly of finger, Camptodactyly, Polyphagia, Dysphagia, Obesity |
OMIM:607872 |
Obesity |
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Obesity, Increased waist to hip ratio |
OMIM:601665 |
Alström Syndrome |
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Obesity, Polyphagia, Truncal obesity, Dorsocervical fat pad |
ORPHA:64 |