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RHOA

ras homolog family member A

HCNC Approved Symbol
RHOA (HGNC:667)
Genomic Coordinates
3:49,359,145 - 49,411,976 (3p21.31)
Synonyms
Rho12, RHOH12, ARH12, ARHA
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

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

Frequently observed phenotypes

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

Blepharophimosis
 1 (100.0%)
Epicanthal fold
 1 (100.0%)
Eyelid ptosis
 1 (100.0%)
Frontal bossing
 1 (100.0%)
Horseshoe kidneys
 1 (100.0%)
RHOA - Gene browser | 3billion