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PRCD

photoreceptor disc component

HCNC Approved Symbol
PRCD (HGNC:32528)
Genomic Coordinates
17:76,527,586 - 76,553,580 (17q25.1)
Synonyms
RP36
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

6Patients

In total, 6 patients were diagnosed with a variant in the PRCD gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Retinitis pigmentosa
 3 (50.0%)
Visual impairment
 2 (33.3%)
Retinal dystrophy
 2 (33.3%)
Adult-onset night blindness
 1 (16.7%)
Pericentral retinitis pigmentosa
 1 (16.7%)
PRCD - Gene browser | 3billion