01
Diseases
Keratoderma, Palmoplantar, Diffuse
keratoderma, palmoplantar, diffuse
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
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Core Information
- Disease Name
- Keratoderma, Palmoplantar, Diffuse
- Standard Disease Name
- keratoderma, palmoplantar, diffuse
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D015776
- OMIM ID
- 144200
- UMLS ID
- C0022584
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:An inherited disorder characterized by the development of keratotic lesions on the palms and soles. It appears in childhood as redness on the palms and soles which progresses to well demarcated, thickened, yellowish and waxy lesions.|MSH2017_2016_08_12:An autosomal dominant disorder characterized by a widely distributed, well-demarcated hyperkeratosis of the palms and soles. There is more than one genotypically distinct form, each of which is clinically similar but histologically distinguishable. Diffuse palmoplantar keratoderma is distinct from palmoplantar keratoderma (KERATODERMA, PALMOPLANTAR), as the former exhibits autosomal dominant inheritance and hyperhidrosis is frequently present.
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Related Targets
target disease8 Targets