CYP4F22 - Gene browser

CYP4F22

cytochrome P450 family 4 subfamily F member 22

HCNC Approved Symbol: CYP4F22 (HGNC:26820)
Genomic Coordinates: 19:15,508,525 - 15,552,317 (19p13.12)
Synonyms: FLJ39501
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

11Patients

In total, 11 patients were diagnosed with a variant in the CYP4F22 gene.

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

011
Patient count

Congenital lamellar ichthyosis: 7 (63.6%)
Patient Count: 7 (63.6%)
% of total patients presenting each phenotype is shown in parentheses.
7 (63.6%)
Congenital ichthyosis: 5 (45.5%)
Patient Count: 5 (45.5%)
% of total patients presenting each phenotype is shown in parentheses.
5 (45.5%)
Ichthyosis: 2 (18.2%)
Patient Count: 2 (18.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (18.2%)
Congenital ichthyosiform erythroderma: 1 (9.1%)
Patient Count: 1 (9.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (9.1%)
Dry skin: 1 (9.1%)
Patient Count: 1 (9.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (9.1%)