Truncal obesity
Symptom Information:
Symptom ID: | HPO:0001956 | |||||||||||||||||
Synonyms: |
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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) 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) |
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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) |