Generalized lipodystrophy
Symptom Information:
Symptom ID: | HPO:0009064 | |||||||||||
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) Abnormality of connective tissue(HPO:0003549) Abnormality of adipose tissue(HPO:0009124) Lipodystrophy(HPO:0009125) Generalized lipodystrophy(HPO:0009064) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin and subcutaneous tissue disorders NEC(MedDRA:10040790) Generalized lipodystrophy(HPO:0009064) |
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Database Frequency: | 17 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Carney complex | (Orphanet:1359) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Familial partial lipodystrophy due to AKT2 mutations | (Orphanet:79085) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
KEPPEN-LUBINSKY SYNDROME | (OMIM:614098) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 | (OMIM:608594) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 | (OMIM:269700) |
Leprechaunism | (Orphanet:508) |
Lipodystrophy - intellectual deficit - deafness | (Orphanet:50811) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Partial acquired lipodystrophy | (Orphanet:79087) |
STIFF SKIN SYNDROME | (OMIM:184900) |
Werner syndrome | (Orphanet:902) |