Disease #03442 (RP43 (retinitis pigmentosa, type 43 (RP43)), OMIM:613810)

Official abbreviation RP43
Name retinitis pigmentosa, type 43 (RP43)
OMIM ID 613810
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene PDE6A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-04-09 15:05:56 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00411352 Fam20 PubMed: Sharon 2020, PubMed: Ben Yosef 2023 family, 1 affected F yes Israel Ethiopia;Jew - - - - RP43 - - PDE6A 1 1 Tamar Ben-Yosef
00436441 4161847 Villafuerte-de la Cruz RA, et al., 2023. Submitted - M likely Mexico Hispanic - - - none RP43 Reduced visual acuity HP:0007663; Nyctalopia HP:0000662; Peripheral visual field loss HP:0007994; Retinitis pigmentosa HP:0000510 PDE6A PDE6A 1 1 Rocio Villafuerte-de la Cruz
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