Disease #02331 (GLC-3B (glaucoma, congenital, primary infantile, type 3B (GLC-3B)), OMIM:600975)

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Official abbreviation	GLC-3B
Name	glaucoma, congenital, primary infantile, type 3B (GLC-3B)
OMIM ID	600975
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	CYP1B1, LTBP2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A