palmoplantar keratoderma, Nagashima type
Keratosis, Nagashima-type is a transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda (see this term)
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palmoplantar keratoderma, Nagashima type
Summary
palmoplantar keratoderma, Nagashima type is a rare disease[1].
Key Facts
- palmoplantar keratoderma, Nagashima type's instance of is recorded as rare disease[2].
- palmoplantar keratoderma, Nagashima type's instance of is recorded as class of disease[3].
- palmoplantar keratoderma, Nagashima type's subclass of is recorded as autosomal recessive isolated diffuse palmoplantar keratoderma[4].
- palmoplantar keratoderma, Nagashima type's OMIM ID is recorded as 615598[5].
- palmoplantar keratoderma, Nagashima type's KEGG ID is recorded as H02264[6].
- palmoplantar keratoderma, Nagashima type's Orphanet ID is recorded as 140966[7].
- palmoplantar keratoderma, Nagashima type's genetic association is recorded as SERPINB7[8].
- palmoplantar keratoderma, Nagashima type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_140966[9].
- palmoplantar keratoderma, Nagashima type's UMLS CUI is recorded as C3810072[10].
- palmoplantar keratoderma, Nagashima type's ICD-10-CM is recorded as Q82.8[11].
- palmoplantar keratoderma, Nagashima type's Mondo ID is recorded as MONDO_0014272[12].
- palmoplantar keratoderma, Nagashima type's ICD-11 ID is recorded as 1288797757[13].
- palmoplantar keratoderma, Nagashima type's UniProt disease ID is recorded as DI-04005[14].