Congenital generalized lipodystrophy
Symptom Information:
Symptom ID: | HPO:0009059 | ||
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) Abnormality of connective tissue(HPO:0003549) Abnormality of adipose tissue(HPO:0009124) Lipodystrophy(HPO:0009125) Congenital generalized lipodystrophy(HPO:0009059) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Lipodystrophy - intellectual deficit - deafness | (Orphanet:50811) |