Disease #02824 (PPCD2 (dystrophy, corneal, posterior polymorphous, type 2 (PPCD-2)), OMIM:609140)

Official abbreviation	PPCD2
Name	dystrophy, corneal, posterior polymorphous, type 2 (PPCD-2)
OMIM ID	609140
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	COL8A2
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD