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GRHL2

grainyhead like transcription factor 2

HCNC Approved Symbol
GRHL2 (HGNC:2799)
Genomic Coordinates
8:101,492,439 - 101,681,200 (8q22.3)
Synonyms
FLJ13782, BOM, DFNA28, TFCP2L3
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Corneal dystrophy, posterior polymorphous, 4
618031AD
Deafness, autosomal dominant 28
608641AD
Ectodermal dysplasia/short stature syndrome
616029AR

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the GRHL2 gene.

Frequently observed phenotypes

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

No Results