Disease #03222 (OPA7 (atrophy, optic, type 7, with/without auditory neuropathy (OPA-7)), OMIM:612989)

Official abbreviation	OPA7
Name	atrophy, optic, type 7, with/without auditory neuropathy (OPA-7)
OMIM ID	612989
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TMEM126A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.

Global Variome shared LOVD