Loss of facial adipose tissue
Symptom Information:
Symptom ID: | HPO:0000292 | |||||
Synonyms: |
|
|||||
Quality: | ||||||
Cross references: |
|
|||||
Is a (Direct Parents): |
|
|||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of facial soft tissue(HPO:0011799) Abnormality of facial adipose tissue(HPO:0000291) Loss of facial adipose tissue(HPO:0000292) Abnormality of connective tissue(HPO:0003549) Abnormality of adipose tissue(HPO:0009124) Abnormality of facial adipose tissue(HPO:0000291) Loss of facial adipose tissue(HPO:0000292) MedDRA: |
|||||
Database Frequency: | 6 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME B | (OMIM:133540) |
Cockayne syndrome | (Orphanet:191) |
LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3,WITH OR WITHOUT GLOMERULONEPHRITIS | (OMIM:613913) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Partial acquired lipodystrophy | (Orphanet:79087) |