CRX - Gene browser

CRX

cone-rod homeobox

HCNC Approved Symbol: CRX (HGNC:2383)
Genomic Coordinates: 19:47,821,937 - 47,843,324 (19q13.33)
Synonyms: CRD, LCA7, OTX3, CORD2
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

21Patients

In total, 21 patients were diagnosed with a variant in the CRX gene.

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

021
Patient count

Decreased visual acuity: 7 (33.3%)
Patient Count: 7 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
7 (33.3%)
Night blindness: 7 (33.3%)
Patient Count: 7 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
7 (33.3%)
Retinitis pigmentosa: 6 (28.6%)
Patient Count: 6 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
6 (28.6%)
Retinal dystrophy: 3 (14.3%)
Patient Count: 3 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
3 (14.3%)
Macular dystrophy: 2 (9.5%)
Patient Count: 2 (9.5%)
% of total patients presenting each phenotype is shown in parentheses.
2 (9.5%)