Disease #02962

Official abbreviation LCA-12
Name Leber congenital amaurosis, type 12 (LCA-12)
OMIM ID 610612
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene RD3
Associated tissues -
Disease features -
Remarks -

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