Abnormal subcutaneous fat tissue distribution

Symptom Information:

Symptom ID: HPO:0007552
Synonyms:
Adipose tissue distribution anomaly [Orphanet:53200]
Abnormal subcutaneous fat tissue distribution [OMIM:Abnormal subcutaneous fat tissue distribution]
Abnormal fat distribution/lipodystrophy [Orphanet:53200]
Quality:
Cross references:
Orphanet:53200 "Abnormal fat distribution/lipodystrophy" [Orphanet:53200]
OMIM: "Abnormal subcutaneous fat tissue distribution" [OMIM:Abnormal subcutaneous fat tissue distribution]
Is a (Direct Parents):
Orphanet Build/stature/longevity anomalies
HPO         Abnormality of subcutaneous fat tissue
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of connective tissue(HPO:0003549)
          Abnormality of adipose tissue(HPO:0009124)
             Abnormality of subcutaneous fat tissue(HPO:0001001)
                Abnormal subcutaneous fat tissue distribution(HPO:0007552)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of subcutaneous fat tissue(HPO:0001001)
                   Abnormal subcutaneous fat tissue distribution(HPO:0007552)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
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)
PMM2-CDG (Orphanet:79318)
Partial acquired lipodystrophy (Orphanet:79087)
Werner syndrome (Orphanet:902)