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FOXL1

forkhead box L1

HCNC Approved Symbol
FOXL1 (HGNC:3817)
Genomic Coordinates
16:86,578,549 - 86,583,478 (16q24.1)
Synonyms
FREAC7, FKH6, FKHL11
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Otosclerosis 11
620576AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the FOXL1 gene.

Frequently observed phenotypes

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

No Results