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

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Official abbreviation	LCA-8
Name	Leber congenital amaurosis, type 8 (LCA-8)
OMIM ID	613835
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
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	N/A