Truncal obesity

Symptom Information:

Symptom ID: HPO:0001956
Synonyms:
Centripetal obesity [HPO:0001956]
Android obesity (disorder) [Orphanet:53150]
Central obesity (disorder) [Orphanet:53150]
Android obesity [Orphanet:53150]
Obesity, Abdominal [Orphanet:53150]
Centripetal obesity [OMIM:Centripetal obesity]
Truncal obesity [OMIM:Truncal obesity]
Truncal obesity [Orphanet:53150]
Central obesity [Orphanet:53150]
Central obesity [MedDRA:10065941]
Abdominal obesity [MedDRA:10065941]
Truncal obesity [MedDRA:10065941]
Abdominal obesity [OMIM:Abdominal obesity]
Central obesity [OMIM:Central obesity]
Truncal obesity (onset in childhood) [OMIM:Truncal obesity (onset in childhood)]
Truncal obesity (rare) [OMIM:Truncal obesity (rare)]
Truncal obesity (variable) [OMIM:Truncal obesity (variable)]
Quality:
Cross references:
Orphanet:53150 "Truncal obesity" [Orphanet:53150]
OMIM: "Centripetal obesity" [OMIM:Centripetal obesity]
OMIM: "Truncal obesity" [OMIM:Truncal obesity]
OMIM: "Abdominal obesity" [OMIM:Abdominal obesity]
OMIM: "Central obesity" [OMIM:Central obesity]
OMIM: "Truncal obesity (onset in childhood)" [OMIM:Truncal obesity (onset in childhood)]
OMIM: "Truncal obesity (rare)" [OMIM:Truncal obesity (rare)]
OMIM: "Truncal obesity (variable)" [OMIM:Truncal obesity (variable)]
UMLS:C0342940 "Android obesity" [Orphanet:53150]
UMLS:C0311277 "Obesity, Abdominal" [Orphanet:53150]
Is a (Direct Parents):
HPO         Obesity
Orphanet Build/stature/longevity anomalies
MedDRA General nutritional disorders NEC
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)
                   Truncal obesity(HPO:0001956)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Appetite and general nutritional disorders(MedDRA:10003018)
       General nutritional disorders NEC(MedDRA:10018067)
          Truncal obesity(HPO:0001956)
Database Frequency: 39 / 7739
Resource:

All diseases associated with this symptom:

ABDOMINAL OBESITY-METABOLIC SYNDROME 3 (OMIM:615812)
ACTH-independent Cushing syndrome (Orphanet:99893)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
Alström syndrome (Orphanet:64)
BARATELA-SCOTT SYNDROME (OMIM:300881)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 10 (OMIM:615987)
Borjeson-Forssman-Lehmann syndrome (Orphanet:127)
Cabezas syndrome (Orphanet:85293)
Cornelia de Lange syndrome (Orphanet:199)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cushing syndrome due to ectopic ACTH secretion (Orphanet:99889)
DESBUQUOIS DYSPLASIA 2 (OMIM:615777)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Growth hormone insensitivity syndrome (Orphanet:181393)
Hypoinsulinemic hypoglycemia and body hemihypertrophy (Orphanet:293964)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit, X-linked - cubitus valgus - dysmorphism (Orphanet:85280)
Laron syndrome (Orphanet:633)
Lysinuric protein intolerance (Orphanet:470)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13 (OMIM:613192)
MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENISSYNDROME (OMIM:610156)
Macrocephaly - spastic paraplegia - dysmorphism (Orphanet:2429)
Megalencephaly (Orphanet:2477)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (OMIM:610489)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 (OMIM:610475)
Polyneuropathy - intellectual deficit - acromicria - premature menopause (Orphanet:2928)
Prader-Willi syndrome (Orphanet:739)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
Primordial short stature - microdontia - opalescent and rootless teeth (Orphanet:46658)
RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION (OMIM:268050)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
TEMPLE SYNDROME (OMIM:616222)
Trichomegaly - retina pigmentary degeneration - dwarfism (Orphanet:3363)
Wilson-Turner syndrome (Orphanet:3459)
Xq27.3q28 duplication syndrome (Orphanet:261483)