Disease #04336 (FECD3 (dystrophy, corneal, Fuchs endothelial, type 3 (FECD-3)), OMIM:613267)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FECD3
Name	dystrophy, corneal, Fuchs endothelial, type 3 (FECD-3)
OMIM ID	613267
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
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	2021-12-10 21:51:32 +01:00 (CET)

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