Obesity
Symptom Information:
Symptom ID: | HPO:0001513 | |||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Growth abnormality(HPO:0001507) Abnormality of body weight(HPO:0004323) Increased body weight(HPO:0004324) Obesity(HPO:0001513) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Appetite and general nutritional disorders(MedDRA:10003018) General nutritional disorders NEC(MedDRA:10018067) Obesity(HPO:0001513) |
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Database Frequency: | 172 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
19p13.12 microdeletion syndrome | (Orphanet:254346) |
1p36 deletion syndrome | (Orphanet:1606) |
22q11.2 deletion syndrome | (Orphanet:567) |
2q37 microdeletion syndrome | (Orphanet:1001) |
3q29 microduplication | (Orphanet:251038) |
48,XXXY syndrome | (Orphanet:96263) |
48,XXYY syndrome | (Orphanet:10) |
6q16 deletion syndrome | (Orphanet:171829) |
8p23.1 microdeletion syndrome | (Orphanet:251071) |
ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:614613) |
APOLIPOPROTEIN E | (OMIM:107741) |
Acanthosis nigricans | (Orphanet:924) |
Achondroplasia | (Orphanet:15) |
Acrocephalosyndactyly | (Orphanet:946) |
Adiposis dolorosa | (Orphanet:36397) |
Albright hereditary osteodystrophy | (Orphanet:665) |
Angelman syndrome | (Orphanet:72) |
Ankylosing vertebral hyperostosis with tylosis | (Orphanet:2206) |
Aromatase deficiency | (Orphanet:91) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Atypical Rett syndrome | (Orphanet:3095) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 18 | (OMIM:615457) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 11 | (OMIM:615988) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Bardet-Biedl syndrome 13 | (OMIM:615990) |
Bardet-Biedl syndrome 14 | (OMIM:615991) |
Bardet-Biedl syndrome 16 | (OMIM:615993) |
Bardet-Biedl syndrome 17 | (OMIM:615994) |
Bardet-Biedl syndrome 18 | (OMIM:615995) |
Bardet-Biedl syndrome 19 | (OMIM:615996) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 3 | (OMIM:600151) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Bardet-Biedl syndrome 5 | (OMIM:615983) |
Bardet-Biedl syndrome 6 | (OMIM:605231) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Bardet-Biedl syndrome 8 | (OMIM:615985) |
Bardet-Biedl syndrome 9 | (OMIM:615986) |
Borjeson-Forssman-Lehmann syndrome | (Orphanet:127) |
Brachydactyly - nystagmus - cerebellar ataxia | (Orphanet:1246) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CLARK-BARAITSER SYNDROME | (OMIM:300602) |
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1 | (OMIM:122000) |
CORTISONE REDUCTASE DEFICIENCY 2 | (OMIM:614662) |
Cabezas syndrome | (Orphanet:85293) |
Carney complex | (Orphanet:1359) |
Carpenter syndrome | (Orphanet:65759) |
Choroideremia - deafness - obesity | (Orphanet:1435) |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | (Orphanet:90794) |
Cogan syndrome | (Orphanet:1467) |
Cohen syndrome | (Orphanet:193) |
Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome | (Orphanet:363741) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Cortisone reductase deficiency 1 | (OMIM:604931) |
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
Cushing disease | (Orphanet:96253) |
DESBUQUOIS DYSPLASIA 1 | (OMIM:251450) |
DIGEORGE SYNDROME | (OMIM:188400) |
Deafness - encephaloneuropathy - obesity - valvulopathy | (Orphanet:254898) |
Desbuquois syndrome | (Orphanet:1425) |
Disorder of sex development - intellectual deficit | (Orphanet:2983) |
Down syndrome | (Orphanet:870) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria | (Orphanet:1035) |
Esophageal adenocarcinoma | (Orphanet:99976) |
Esophageal carcinoma | (Orphanet:70482) |
HALOTHANE HEPATITIS | (OMIM:234350) |
HELSMOORTEL-VAN DER AA SYNDROME | (OMIM:615873) |
HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA | (OMIM:610628) |
Hemochromatosis type 3 | (Orphanet:225123) |
Hernandez-Aguirre Negrete syndrome | (Orphanet:2139) |
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly | (Orphanet:2180) |
Hydrocephalus - obesity - hypogonadism | (Orphanet:2183) |
Hyperandrogenism due to cortisone reductase deficiency | (Orphanet:168588) |
Hyperinsulinism-hyperammonemia syndrome | (Orphanet:35878) |
Hypogonadism - mitral valve prolapse - intellectual deficit | (Orphanet:2233) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Intellectual deficit, X-linked - hypogonadism - ichthyosis - obesity - short stature | (Orphanet:85331) |
Intellectual deficit, X-linked - precocious puberty - obesity | (Orphanet:85318) |
Intellectual deficit, X-linked - short stature - obesity | (Orphanet:3055) |
Intellectual deficit, X-linked, Shashi type | (Orphanet:85286) |
Intellectual deficit, X-linked, Stevenson type | (Orphanet:85325) |
Kabuki syndrome | (Orphanet:2322) |
Kallmann syndrome | (Orphanet:478) |
Kleefstra syndrome | (Orphanet:261494) |
Kleefstra syndrome due to 9q34 microdeletion | (Orphanet:96147) |
Laurence-Moon syndrome | (Orphanet:2377) |
Lethal polymalformative syndrome, Boissel type | (Orphanet:210144) |
Lipedema | (Orphanet:77243) |
MACROSOMIA ADIPOSA CONGENITA | (OMIM:248100) |
MEHMO syndrome | (Orphanet:85282) |
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTICFEATURES | (OMIM:613670) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 | (OMIM:614202) |
MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES | (OMIM:606772) |
MENTAL RETARDATION, X-LINKED 91 | (OMIM:300577) |
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA | (OMIM:608624) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE) | (OMIM:615418) |
MOMO syndrome | (Orphanet:2563) |
MORBID OBESITY AND SPERMATOGENIC FAILURE | (OMIM:615703) |
Macrocephaly-autism syndrome | (Orphanet:210548) |
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies | (Orphanet:2234) |
Maturity-onset diabetes of the young, type 11 | (OMIM:613375) |
Maturity-onset diabetes of the young, type 2 | (OMIM:125851) |
Maturity-onset diabetes of the young, type 4 | (OMIM:606392) |
Maturity-onset diabetes of the young, type 6 | (OMIM:606394) |
McKusick-Kaufman syndrome | (Orphanet:2473) |
Metaphyseal dysostosis - intellectual deficit - conductive deafness | (Orphanet:2502) |
Microduplication Xp11.22-p11.23 syndrome | (Orphanet:217377) |
Monosomy 22q13 | (Orphanet:48652) |
Morgagni-Stewart-Morel syndrome | (Orphanet:77296) |
Mulibrey nanism | (Orphanet:2576) |
Multiple epiphyseal dysplasia, Al-Gazali type | (Orphanet:166024) |
Myhre syndrome | (Orphanet:2588) |
NARCOLEPSY 7 | (OMIM:614250) |
Narcolepsy-cataplexy | (Orphanet:2073) |
Nephronophthisis 15 | (OMIM:614845) |
OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY | (OMIM:613886) |
OBESITY-HYPOVENTILATION SYNDROME | (OMIM:257500) |
Obesity - colitis - hypothyroidism - cardiac hypertrophy - developmental delay | (Orphanet:88643) |
Obesity due to MC3R deficiency | (Orphanet:217031) |
Obesity due to congenital leptin deficiency | (Orphanet:66628) |
Obesity due to leptin receptor gene deficiency | (Orphanet:179494) |
Obesity due to melanocortin 4 receptor deficiency | (Orphanet:71529) |
Obesity due to pro-opiomelanocortin deficiency | (Orphanet:71526) |
Obesity due to prohormone convertase I deficiency | (Orphanet:71528) |
Osteoporosis - pseudoglioma | (Orphanet:2788) |
POLYCYSTIC OVARY SYNDROME 1 | (OMIM:184700) |
PROLACTIN DEFICIENCY WITH OBESITY AND ENLARGED TESTES | (OMIM:264120) |
Posterior polymorphous corneal dystrophy | (Orphanet:98973) |
Prader-Willi syndrome | (Orphanet:739) |
Proximal 16p11.2 microdeletion syndrome | (Orphanet:261197) |
Pseudohypoparathyroidism type 1A | (Orphanet:79443) |
Pseudohypoparathyroidism type 1B | (Orphanet:94089) |
Pseudohypoparathyroidism type 1C | (Orphanet:79444) |
Pseudopseudohypoparathyroidism | (Orphanet:79445) |
RETINAL DYSTROPHY AND OBESITY | (OMIM:616188) |
Retinitis pigmentosa | (Orphanet:791) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |
Retinohepatoendocrinologic syndrome | (Orphanet:3087) |
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion | (Orphanet:353281) |
SCHAAF-YANG SYNDROME | (OMIM:615547) |
SHORT STATURE-OBESITY SYNDROME | (OMIM:269870) |
SPERMATOGENIC FAILURE, X-LINKED, 1 | (OMIM:305700) |
Secondary polycythemia | (Orphanet:98428) |
Senior-Loken syndrome 9 | (OMIM:616629) |
Septo-optic dysplasia | (Orphanet:3157) |
Short-rib thoracic dysplasia 10 with or without polydactyly | (OMIM:615630) |
Short-rib thoracic dysplasia 11 with or without polydactyly | (OMIM:615633) |
Smith-Magenis syndrome | (Orphanet:819) |
Sotos syndrome | (Orphanet:821) |
Subaortic stenosis - short stature | (Orphanet:3191) |
Summitt syndrome | (Orphanet:3210) |
Symptomatic form of Coffin-Lowry syndrome in female carriers | (Orphanet:276630) |
Syndromic X-linked intellectual deficit 7 | (Orphanet:85274) |
TRIGLYCERIDE STORAGE DISEASE, TYPE II | (OMIM:190430) |
Tetrasomy 12p | (Orphanet:884) |
Thumb stiffness - brachydactyly - intellectual deficit | (Orphanet:1078) |
Trisomy 5p | (Orphanet:1742) |
Ulnar-mammary syndrome | (Orphanet:3138) |
Urban-Rogers-Meyer syndrome | (Orphanet:3409) |
WAGR syndrome | (Orphanet:893) |
WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME | (OMIM:194072) |
Williams syndrome | (Orphanet:904) |
Wilson-Turner syndrome | (Orphanet:3459) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |