Disease #03456

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 0
Phenotype entries for this disease 0
Associated with 1 gene CRB1
Associated tissues -
Disease features -
Remarks -

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