Disease #03226 (FNEPPK1 (keratoderma, palmoplantar, nonepidermolytic, focal, type 1 (FNEPPK-1)), OMIM:613000)

Official abbreviation FNEPPK1
Name keratoderma, palmoplantar, nonepidermolytic, focal, type 1 (FNEPPK-1)
OMIM ID 613000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene KRT16
Associated tissues -
Disease features -
Remarks -