Disease #03671 (CORD16;RP64 (dystrophy, cone-rod, type 16 (CORD16), retinitis pigmentosa, type 64 (RP64)), OMIM:614500)

Official abbreviation CORD16;RP64
Name dystrophy, cone-rod, type 16 (CORD16), retinitis pigmentosa, type 64 (RP64)
OMIM ID 614500
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene C8orf37
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-08-30 11:04:14 +02:00 (CEST)

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