Disease #03440 (RP40 (retinitis pigmentosa, type 40 (RP40)), OMIM:613801)

Official abbreviation RP40
Name retinitis pigmentosa, type 40 (RP40)
OMIM ID 613801
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 2
Associated with 1 gene PDE6B
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

4 entries on 1 page. Showing entries 1 - 4.
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00382137 261 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - RP40 retinal dystrophy; MIM, 613801 or 163500 PDE6B PDE6B, RPE65 4 1 LOVD
00411342 Fam15 PubMed: Sharon 2020, PubMed: Ben Yosef 2023 family, 1 affected F - Israel Ethiopia;Jew - - - - RP40 - - PDE6B 1 1 Tamar Ben-Yosef
00411343 Fam16 PubMed: Ben Yosef 2023 family, 1 affected M yes Israel Ethiopia;Jew - - - - RP40 - - PDE6B 1 1 Tamar Ben-Yosef
00412655 patient - - F yes Pakistan South Asian - - - - RP40 Retinitis pigmentosa PDE6B PDE6B 1 4 Khadim Shah
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