Disease #04336 (FECD-3 (dystrophy, corneal, Fuchs endothelial, type 3 (FECD-3)), OMIM:613267)

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	Curator: Johan T. den Dunnen

Official abbreviation	FECD-3
Name	dystrophy, corneal, Fuchs endothelial, type 3 (FECD-3)
OMIM ID	613267
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TCF4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-22 17:29:12 +02:00 (CEST)
Date last edited	N/A