FGF13

fibroblast growth factor 13

HCNC Approved Symbol

FGF13 (HGNC:3670)

Genomic Coordinates

23:138,614,727 - 139,205,023 (Xq26.3-q27.1)

Synonyms

FHF2, FGF2, FLJ30672, LINC00889

Disease Associations

This gene is associated with the following 2 diseases in OMIM.

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Disease NameOMIM IDInheritance

Developmental and epileptic encephalopathy 90

301058X-linked dominant; X-linked recessive

Intellectual developmental disorder, X-linked 110

301095X-linked recessive