FGA - Gene browser

FGA

fibrinogen alpha chain

HCNC Approved Symbol: FGA (HGNC:3661)
Genomic Coordinates: 4:154,583,126 - 154,590,742 (4q31.3)
Synonyms
Disease Associations: This gene is associated with the following 4 diseases in OMIM.

6Patients

In total, 6 patients were diagnosed with a variant in the FGA gene.

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

06
Patient count

Low fibrinogen level: 2 (33.3%)
Patient Count: 2 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (33.3%)
Lymphadenopathy: 2 (33.3%)
Patient Count: 2 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (33.3%)
Nephrotic syndrome: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Nephrotic syndrome, steroid-resistant: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Steroid-resistant nephrotic syndrome: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)