FGG - Gene browser | 3billion

FGG

FGG

fibrinogen gamma chain

HCNC Approved Symbol: FGG (HGNC:3694)
Genomic Coordinates: 4:154,604,136 - 154,612,656 (4q32.1)
Synonyms
Disease Associations: This gene is associated with the following 4 diseases in OMIM.

Diagnosed Cases

1Patient

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

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Hepatitis: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Hypertriglyceridemia: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Hypofibrinogenemia: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

FGG - Gene browser | 3billion