Partial lipodystrophy
Symptom Information:
Symptom ID: | MedDRA:10053857 | |||
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Is a (Whole tree): |
HPO:
MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin and subcutaneous tissue disorders NEC(MedDRA:10040790) Generalized lipodystrophy(HPO:0009064) Partial lipodystrophy(MedDRA:10053857) |
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Database Frequency: | 8 / 7739 | |||
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All diseases associated with this symptom:
CANDLE syndrome | (Orphanet:325004) |
Familial partial lipodystrophy associated with PLIN1 mutations | (Orphanet:280356) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
JMP syndrome | (Orphanet:324999) |
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5 | (OMIM:615238) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Proteasome disability syndrome | (Orphanet:324977) |