FHOD3 - Gene browser

FHOD3

formin homology 2 domain containing 3

HCNC Approved Symbol: FHOD3 (HGNC:26178)
Genomic Coordinates: 18:36,297,713 - 36,780,220 (18q12.2)
Synonyms: FHOS2, KIAA1695, FLJ22297, FLJ22717
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

5Patients

In total, 5 patients were diagnosed with a variant in the FHOD3 gene.

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

05
Patient count

Hypertrophic cardiomyopathy: 3 (60.0%)
Patient Count: 3 (60.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (60.0%)
Heart failure: 2 (40.0%)
Patient Count: 2 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (40.0%)
Left ventricular hypertrophy: 2 (40.0%)
Patient Count: 2 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (40.0%)
Bilateral superior vena cava with bridging vein: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)
Delayed speech and language development: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)