Disease #05687 (RP75 (retinitis pigmentosa, type 75 (RP75)), OMIM:617023)

Official abbreviation RP75
Name retinitis pigmentosa, type 75 (RP75)
OMIM ID 617023
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene AGBL5
Associated tissues -
Disease features -
Remarks -

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