FGB - Gene browser

FGB

fibrinogen beta chain

HCNC Approved Symbol: FGB (HGNC:3662)
Genomic Coordinates: 4:154,562,980 - 154,572,807 (4q31.3)
Synonyms
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

1Patient

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

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

01
Patient count

Abnormal umbilical stump bleeding: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Bleeding from mouth: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Budd-chiari syndrome: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Liver cirrhosis: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Prolonged activated partial thromboplastin time: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)