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

Global Variome shared LOVD

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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	-
Phenotype entries for this disease	-
Associated with 1 gene	GJA1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2015-12-08 23:53:05 +01:00 (CET)

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