Disease #00186 (MCOPS-2 (microphthalmia, syndromic, type 2 (MCOPS-2)), OMIM:300166)

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	Curator: Johan T. den Dunnen

Official abbreviation	MCOPS-2
Name	microphthalmia, syndromic, type 2 (MCOPS-2)
OMIM ID	300166
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	BCOR
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-09-05 15:25:12 +02:00 (CEST)
Date last edited	N/A