Disease #04410 (MGC-1 (megalocornea, type 1, X-linked (MGC-1)), OMIM:309300)

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Official abbreviation	MGC-1
Name	megalocornea, type 1, X-linked (MGC-1)
OMIM ID	309300
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CHRDL1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	N/A