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Autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature

MedGen UID:: 1842766
•Concept ID:: C5680345
•: Disease or Syndrome

Synonym:	Autosomal dominant disease associated with focal palmoplantar hyperkeratosis as a major feature

Orphanet:	ORPHA98353

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GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVAutosomal dominant disease associated with focal palmoplantar keratoderma as a major feature

Autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature

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Autosomal dominant disease associated with focal palmoplantar keratoderma as a m...
Autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature

MedGen
RB195_004349 [Necator americanus]
RB195_004349 [Necator americanus]
Gene ID:25352357

Gene

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