Abnormal subcutaneous fat tissue distribution
Symptom Information:
Symptom ID: | HPO:0007552 | ||||
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 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) 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) MedDRA: |
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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) |