Disease #03946 (RP82 (retinitis pigmentosa, with/without situs inversus (RP82)), OMIM:615434)

Official abbreviation RP82
Name retinitis pigmentosa, with/without situs inversus (RP82)
OMIM ID 615434
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 5
Associated with 1 gene ARL2BP
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2019-12-17 16:21:56 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00145073 7297-02348 - 4-generation family, 3 affected (2 males, 1 female), unaffected consanguineous deceased parents F yes China Asian-Chinese >41y - yes none RP82 HP:0007663, reduced visual acuity; HP:0000505, visual impairment; HP:0007722, retinal pigment epithelial atrophy; HP:0007843, attenuation of retinal blood vessels; HP:0007737; bone spicule pigmentation of the retina; HP:0001133, constriction of peripheral visual field; HP:0000662, nyctalopia ABCA4 ABCA4 1 3 Hao Deng
00154483 MOL0100PatII1/2 PubMed: Bandah-Rozenfeld 2010, PubMed: Kimchi 2018 family, 2 affected (F, M) F;M - Morocco Jewish - - - - RP82 ... FAM161A FAM161A 1 2 Dror Sharon
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