Disease #04486 (PPKCA1 (keratoderma, palmoplantar, with congenital alopecia, type 1 (PPKCA-1)), OMIM:104100)

Official abbreviation PPKCA1
Name keratoderma, palmoplantar, with congenital alopecia, type 1 (PPKCA-1)
OMIM ID 104100
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene GJA1
Associated tissues -
Disease features -
Remarks -