Disease #03296 (FECD-4 (dystrophy, corneal, Fuchs endothelial, type 4 (FECD-4)), OMIM:613268)

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Official abbreviation	FECD-4
Name	dystrophy, corneal, Fuchs endothelial, type 4 (FECD-4)
OMIM ID	613268
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC4A11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A