Congenital generalized lipodystrophy

Symptom Information:

Symptom ID: HPO:0009059
Synonyms:
Congenital generalized lipodystrophy [OMIM:Congenital generalized lipodystrophy]
Quality:
Cross references:
OMIM: "Congenital generalized lipodystrophy" [OMIM:Congenital generalized lipodystrophy]
Is a (Direct Parents):
HPO         Lipodystrophy
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:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Lipodystrophy - intellectual deficit - deafness (Orphanet:50811)