Disease #00702 (LCA-10 (Leber congenital amaurosis, type 10 (LCA-10)), OMIM:611755)

Official abbreviation LCA-10
Name Leber congenital amaurosis, type 10 (LCA-10)
OMIM ID 611755
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 0
Associated with 1 gene CEP290
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Individuals

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00269432 - - - M no Korea Asian 24y 0 - - JBTS-3, LCA-10 - AHI1, AIPL1, BBS1, CC2D2A, CEP290, CRB1, CRX, GUCY2D, NMNAT1, POLG, RPE65, RPGRIP1, SPATA7, TBX1, WDR19 AHI1 1 1 Jinu Han
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