Disease #05499 (OPA5 (atrophy, optic, type 5 (OPA-5)), OMIM:610708)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	OPA5
Name	atrophy, optic, type 5 (OPA-5)
OMIM ID	610708
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DNM1L
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2018-11-05 20:03:18 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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