Disease #03457 (LCA11 (Leber congenital amaurosis, type 11 (LCA-11)), OMIM:613837)

Official abbreviation LCA11
Name Leber congenital amaurosis, type 11 (LCA-11)
OMIM ID 613837
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
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Associated with 1 gene IMPDH1
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