Obesity

Symptom Information:

Symptom ID: HPO:0001513
Synonyms:
Obese (finding) [Orphanet:53100]
Obesity (disorder) [Orphanet:53100]
Obesity [Orphanet:53100]
Obesity [OMIM:Obesity]
Generalized obesity [Orphanet:53100]
Obesity [MedDRA:10029883]
Adiposis [MedDRA:10029883]
Gross obesity [MedDRA:10029883]
Morbid obesity [MedDRA:10029883]
Obesity and other hyperalimentation [MedDRA:10029883]
Obesity, unspecified [MedDRA:10029883]
Other obesity and hyperalimentation [MedDRA:10029883]
Adipositas [MedDRA:10029883]
Adipositas per magna [MedDRA:10029883]
Gross obesity [OMIM:Gross obesity]
Obesity (1 patient) [OMIM:Obesity (1 patient)]
Obesity (35% of adults) [OMIM:Obesity (35% of adults)]
Obesity (after infancy) [OMIM:Obesity (after infancy)]
Obesity (in 1 family) [OMIM:Obesity (in 1 family)]
Obesity (in some patients) [OMIM:Obesity (in some patients)]
Obesity (in some) [OMIM:Obesity (in some)]
Obesity (less common) [OMIM:Obesity (less common)]
Obesity (older children) [OMIM:Obesity (older children)]
Quality:
Cross references:
Orphanet:53100 "Generalized obesity" [Orphanet:53100]
OMIM: "Obesity" [OMIM:Obesity]
OMIM: "Gross obesity" [OMIM:Gross obesity]
OMIM: "Obesity (1 patient)" [OMIM:Obesity (1 patient)]
OMIM: "Obesity (35% of adults)" [OMIM:Obesity (35% of adults)]
OMIM: "Obesity (after infancy)" [OMIM:Obesity (after infancy)]
OMIM: "Obesity (in 1 family)" [OMIM:Obesity (in 1 family)]
OMIM: "Obesity (in some patients)" [OMIM:Obesity (in some patients)]
OMIM: "Obesity (in some)" [OMIM:Obesity (in some)]
OMIM: "Obesity (less common)" [OMIM:Obesity (less common)]
OMIM: "Obesity (older children)" [OMIM:Obesity (older children)]
UMLS:C1963185 "Obesity" [HPO:0001513]
UMLS:C0028754 "Obesity" [Orphanet:53100]
Is a (Direct Parents):
MedDRA General nutritional disorders NEC
Orphanet Build/stature/longevity anomalies
HPO         Increased body weight
HPO         Abdominal obesity
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)
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)