Disease #02387 (RP19 (retinitis pigmentosa, type 19 (RP19)), OMIM:601718)

Official abbreviation RP19
Name retinitis pigmentosa, type 19 (RP19)
OMIM ID 601718
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 8
Phenotype entries for this disease 6
Associated with 1 gene ABCA4
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

8 entries on 1 page. Showing entries 1 - 8.
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00320328 SRF1118 Zixi Sun 2020, submitted - F - China - - - - - RP19 - - ABCA4 2 1 Zixi Sun
00320329 SRF1031 Zixi Sun 2020, submitted - M - China - - - - - RP19 - - ABCA4 1 1 Zixi Sun
00320330 1800 Zixi Sun 2020, submitted - M - China - - - - - RP19 - - ABCA4 1 1 Zixi Sun
00320331 1870 Zixi Sun 2020, submitted - F - China - - - - - RP19 - - ABCA4 2 1 Zixi Sun
00324518 A1 - - F no China - >34y - yes none RP19 - ABCA4, AHI1 ABCA4, AHI1 4 1 Qing Zhu
00326994 Hongyang-ARL3 - - M - China - - - - - RP19 rod-cone dystrophy ARL3 ARL3 2 1 Leming Fu
00408787 - - - - - Mexico - - - - - RP19 - ABCA4 ABCA4 1 1 Nancy Xilotl de Jesús
00465252 Pat1 - - M yes China Asian - - - - RP19 - ABCA4 ABCA4 1 1 Jihong Luo
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