Disease #06793 (PPCD4 (Corneal dystrophy, posterior polymorphous, 4), OMIM:618031)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	PPCD4
Name	Corneal dystrophy, posterior polymorphous, 4
OMIM ID	618031
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GRHL2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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