Disease #00702 (LCA10 (Leber congenital amaurosis, type 10 (LCA-10)), OMIM:611755)

Official abbreviation LCA10
Name Leber congenital amaurosis, type 10 (LCA-10)
OMIM ID 611755
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene CEP290
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00269432 - - - M no Korea Asian 24y - - - JBTS3, LCA10 - AHI1, AIPL1, BBS1, CC2D2A, CEP290, CRB1, CRX, GUCY2D, NMNAT1, POLG, RPE65, RPGRIP1, SPATA7, TBX1, WDR19 AHI1 1 1 Jinu Han
00436606 3446878 Villafuerte-de la Cruz RA, et al., 2023. Submitted - F no Mexico Hispanic - - - NONE LCA10 Blindness HP:0000618, Retinitis pigmentosa HP:0000510 CEP290 CEP290 1 1 Rocio Villafuerte-de la Cruz
00436736 3446878 Villafuerte-de la Cruz RA, et al., 2023. Submitted - F no Mexico Hispanic - - - NONE LCA10 HP: 0007875 Congenital Amaurosis CEP290 CEP290 2 1 Rocio Villafuerte-de la Cruz
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