Disease #03087

Official abbreviation RP-41
Name retinitis pigmentosa, type 41 (RP-41)
OMIM ID 612095
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PROM1
Associated tissues -
Disease features -
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00032824 - PubMed: Maw 2000 - - - India Indian - 0 - - RP-41 retinal degeneration PROM1 PROM1 1 4 Pascal Escher
00032825 - PubMed: Zhang 2007 - - - Pakistan Pundjab - 0 - - RP-41 retinal degeneration PROM1 PROM1 1 6 Pascal Escher
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