Loss of facial adipose tissue

Symptom Information:

Symptom ID: HPO:0000292
Synonyms:
Loss of facial subcutaneous adipose tissue [HPO:0000292]
Loss of subcutaneous adipose tissue from face [HPO:0000292]
Loss of facial adipose tissue [OMIM:Loss of facial adipose tissue]
Loss of facial subcutaneous adipose tissue [OMIM:Loss of facial subcutaneous adipose tissue]
Loss of subcutaneous adipose tissue from face [OMIM:Loss of subcutaneous adipose tissue from face]
Quality:
Cross references:
OMIM: "Loss of facial adipose tissue" [OMIM:Loss of facial adipose tissue]
OMIM: "Loss of facial subcutaneous adipose tissue" [OMIM:Loss of facial subcutaneous adipose tissue]
OMIM: "Loss of subcutaneous adipose tissue from face" [OMIM:Loss of subcutaneous adipose tissue from face]
Is a (Direct Parents):
HPO         Abnormality of facial adipose tissue
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)