Generalized lipodystrophy

Symptom Information:

Symptom ID: HPO:0009064
Synonyms:
Lipodystrophy, generalized [HPO:0009064]
Lipodystrophy [Orphanet:53200]
Lipodystrophy (disorder) [Orphanet:53200]
Generalized lipodystrophy [OMIM:Generalized lipodystrophy]
Abnormal fat distribution/lipodystrophy [Orphanet:53200]
Lipodystrophy acquired [MedDRA:10049287]
Lipodystrophy [MedDRA:10049287]
Flat buttocks [MedDRA:10049287]
Peripheral lipodystrophy [MedDRA:10049287]
Lipodystrophy (in some patients) [OMIM:Lipodystrophy (in some patients)]
Lipodystrophies [MedDRA:10024606]
Quality:
Cross references:
HPO:0009125 "Lipodystrophy" [Orphanet:53200]
Orphanet:53200 "Abnormal fat distribution/lipodystrophy" [Orphanet:53200]
OMIM: "Generalized lipodystrophy" [OMIM:Generalized lipodystrophy]
OMIM: "Lipodystrophy (in some patients)" [OMIM:Lipodystrophy (in some patients)]
UMLS:C0023787 "Lipodystrophy" [Orphanet:53200]
Is a (Direct Parents):
MedDRA Skin and subcutaneous tissue disorders NEC
Orphanet Abnormal subcutaneous fat tissue distribution
HPO         Lipodystrophy
Orphanet Build/stature/longevity anomalies
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)
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)