Disease #00460 (CDGG-1 (dystrophy, corneal, Groenouw type I (CDGG-1)), OMIM:121900)

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	Curator: Johan T. den Dunnen

Official abbreviation	CDGG-1
Name	dystrophy, corneal, Groenouw type I (CDGG-1)
OMIM ID	121900
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TGFBI
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-07-21 14:25:53 +02:00 (CEST)
Date last edited	N/A