Generalized abnormality of skin

Symptom Information:

Symptom ID: HPO:0011354
Generalised abnormality of skin [HPO:0011354]
Skin anomaly [Orphanet:23000]
Skin Abnormalities [Orphanet:23000]
Anomalies of skin, subcutaneous tissue and mucosae [Orphanet:23000]
Skin and mucosa anomaly [Orphanet:23000]
Subcutaneous tissue anomaly [Orphanet:23000]
Mucous membrane disorder [MedDRA:10028133]
Mucosa anomaly [Orphanet:23000]
Disorder of mucous membrane (disorder) [Orphanet:23000]
Disease of mucous membrane [Orphanet:23000]
Cross references:
HPO:0000951 "Abnormality of the skin" [Orphanet:23000]
Orphanet:23000 "Anomalies of skin, subcutaneous tissue and mucosae" [Orphanet:23000]
UMLS:C0037268 "Skin Abnormalities" [Orphanet:23000]
UMLS:C0151785 "Disease of mucous membrane" [Orphanet:23000]
Is a (Direct Parents):
HPO         Abnormality of the skin
Orphanet Abnormality of the skin
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
Database Frequency: 7 / 7739

All diseases associated with this symptom:

Bloom syndrome (Orphanet:125)
CADASIL (Orphanet:136)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Partial acquired lipodystrophy (Orphanet:79087)
Rosaï-Dorfman disease (Orphanet:158014)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Tyrosinemia type 2 (Orphanet:28378)