Congenital localized absence of skin
Symptom Information:
Symptom ID: | HPO:0007383 | ||
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) Localized skin lesion(HPO:0011355) Aplasia/Hypoplasia of the skin(HPO:0008065) Congenital localized absence of skin(HPO:0007383) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN ANDDEFORMITY OF NAILS | (OMIM:132000) |
Junctional epidermolysis bullosa, Herlitz type | (Orphanet:79404) |