01
Diseases
Autosomal Dominant Palmoplantar Keratoderma And Congenital Alopecia
autosomal dominant palmoplantar keratoderma and congenital alopecia
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 1
Basic Information
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Core Information
- Disease Name
- Autosomal Dominant Palmoplantar Keratoderma And Congenital Alopecia
- Standard Disease Name
- autosomal dominant palmoplantar keratoderma and congenital alopecia
- MeSH Tree
- No data
- ICD-10
- Q82.8
Identifiers
- DO ID
- No data
- MeSH ID
- C537050
- OMIM ID
- 104100
- UMLS ID
- C1863093
- HPO ID
- No data
Description and Extensions
- Description
- Autosomal dominant palmoplantar keratoderma with congenital alopecia (PPK-CA) is a rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma, without othe
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