Disease #02440 (RP25 (retinitis pigmentosa, type 25 (RP25)), OMIM:602772)

Official abbreviation RP25
Name retinitis pigmentosa, type 25 (RP25)
OMIM ID 602772
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene EYS
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

2 entries on 1 page. Showing entries 1 - 2.
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00372757 175713 - - - - - - - - - - RP25 retinitis pigmentosa since the age of 30; visual loss on both eyes, bony tubercles, optic atrophy, macular degeneration. EYS EYS 1 1 Andreas Laner
00465319 Case #2 - - F likely Mexico Latin american - - - - RP25 - - EYS 1 1 Vianey Ordoñez-Labastida
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