Disease #07051 (OPA16 (atrophy, optic, type 16), OMIM:620629)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OPA16
Name	atrophy, optic, type 16
OMIM ID	620629
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MECR
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-12-23 19:30:10 +01:00 (CET)
Date last edited	N/A

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