DSG4 - Gene browser | 3billion

DSG4

DSG4

desmoglein 4

HCNC Approved Symbol: DSG4 (HGNC:21307)
Genomic Coordinates: 18:31,376,777 - 31,414,909 (18q12.1)
Synonyms: CDHF13, LAH
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the DSG4 gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Alopecia: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Poor vision: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

DSG4 - Gene browser | 3billion