Disease #02803 (MYP6 (myopia, type 6 (MYP6)), OMIM:608908)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MYP6
Name	myopia, type 6 (MYP6)
OMIM ID	608908
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SCO2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-07-23 10:35:51 +02:00 (CEST)

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