CDHR1 - Gene browser

CDHR1

cadherin related family member 1

HCNC Approved Symbol: CDHR1 (HGNC:14550)
Genomic Coordinates: 10:84,194,537 - 84,219,621 (10q23.1)
Synonyms: KIAA1775, CORD15, RP65, PCDH21
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

11Patients

In total, 11 patients were diagnosed with a variant in the CDHR1 gene.

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

011
Patient count

Macular dystrophy: 4 (36.4%)
Patient Count: 4 (36.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (36.4%)
Retinitis pigmentosa: 3 (27.3%)
Patient Count: 3 (27.3%)
% of total patients presenting each phenotype is shown in parentheses.
3 (27.3%)
Decreased visual acuity: 2 (18.2%)
Patient Count: 2 (18.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (18.2%)
Night blindness: 2 (18.2%)
Patient Count: 2 (18.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (18.2%)
Visual disturbances: 2 (18.2%)
Patient Count: 2 (18.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (18.2%)