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FGF12

fibroblast growth factor 12

HCNC Approved Symbol
FGF12 (HGNC:3668)
Genomic Coordinates
3:192,139,390 - 192,727,541 (3q28-q29)
Synonyms
FHF1, FGF12B
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Developmental and epileptic encephalopathy 47
617166AD

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the FGF12 gene.

Frequently observed phenotypes

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

No Results