Disease #00888 (RP55 (retinitis pigmentosa, type 55 (RP55)), OMIM:613575)

Official abbreviation RP55
Name retinitis pigmentosa, type 55 (RP55)
OMIM ID 613575
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ARL6
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-04-09 15:05:56 +02:00 (CEST)

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