Disease #06968 (LHONAR (Leber hereditary optic neuropathy, autosomal recessive autosomal recessive), OMIM:619382)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	LHONAR
Name	Leber hereditary optic neuropathy, autosomal recessive autosomal recessive
OMIM ID	619382
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DNAJC30
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-09-29 11:04:16 +02:00 (CEST)
Date last edited	2022-09-29 11:05:00 +02:00 (CEST)

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