Disease #07144 (OPA12 (optic atrophy, type 12), OMIM:618977)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OPA12
Name	optic atrophy, type 12
OMIM ID	618977
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	AFG3L2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-12-23 17:35:43 +01:00 (CET)
Date last edited	N/A

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