Disease #01541 (RP1 (retinitis pigmentosa, type 1 (RP1)), OMIM:180100)

Official abbreviation RP1
Name retinitis pigmentosa, type 1 (RP1)
OMIM ID 180100
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene RP1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-05-21 11:46:23 +02:00 (CEST)


Individuals

1 entry on 1 page. Showing entry 1.
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00445399 - - - F yes (Iran) - - - - - RP1 - RP1 RP1 1 1 Mostafa Neissi
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