hepatic fibrinogen storage disease
MONDO:7770747Mondo
Findings
No curated finding names hepatic fibrinogen storage disease yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An autosomal dominant disorder characterized by hypofibrinogenemia and variable liver disease (ranging from asymptomatic transaminase elevation to cirrhosis), caused by variants in FGG that lead to retention of variant fibrinogen as eosinophilic inclusions within the hepatocellular endoplasmic reticulum.
Definition from the Mondo Disease Ontology (MONDO:7770747), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
4 names
Resolves to: hepatic fibrinogen storage disease
- Also called
- hepatocellular fibrinogen storage diseasehereditary hypofibrinogenemia with hepatic storageHFSDHHHS