01
Diseases
Keratoderma, Palmoplantar, Epidermolytic
keratoderma, palmoplantar, epidermolytic
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
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Core Information
- Disease Name
- Keratoderma, Palmoplantar, Epidermolytic
- Standard Disease Name
- keratoderma, palmoplantar, epidermolytic
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D053546
- OMIM ID
- 144200|139350|607606|MTHU036853
- UMLS ID
- C1721006
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:A genetic skin disorder caused by mutations in the KRT9 gene. It is characterized by hyperkeratosis in the palms and soles resulting in abnormal thickening of the skin in these areas.|MSH2017_2016_08_12:An autosomal dominant hereditary skin disease characterized by epidermolytic hyperkeratosis that is strictly confined to the palms and soles. It has been associated with mutations in the gene that codes for KERATIN-9.
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Related Targets
target disease8 Targets