Generalized abnormality of skin
Symptom Information:
Symptom ID: | HPO:0011354 | ||||||||||
Synonyms: |
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Cross references: |
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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) MedDRA: |
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Database Frequency: | 7 / 7739 | ||||||||||
Resource: |
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) |