Disease #03456 (LCA8 (Leber congenital amaurosis, type 8), OMIM:613835)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	LCA8
Name	Leber congenital amaurosis, type 8
OMIM ID	613835
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CRB1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2022-10-27 14:54:46 +02:00 (CEST)

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