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Familial dysfibrinogenemia
1 OMIM reference -
3 associated genes
32 connected diseases
6 signs/symptoms
Disease Type of connection
Familial afibrinogenemia
Familial hypodysfibrinogenemia
Familial hypofibrinogenemia
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
Congenital factor XIII deficiency
Fibronectin glomerulopathy
Autosomal dominant macrothrombocytopenia
Fetal and neonatal alloimmune thrombocytopenia
Glanzmann thrombasthenia
Cerebral sinovenous thrombosis
Congenital factor II deficiency
Synpolydactyly type 2
Essential thrombocythemia
Myelofibrosis with myeloid metaplasia
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Apolipoprotein A-I deficiency
Congenital analbuminemia
Familial renal amyloidosis due to Apolipoprotein AI variant
Primary systemic amyloidosis
Chronic mucocutaneous candidiasis
Amyotrophic lateral sclerosis
B-cell chronic lymphocytic leukemia
Cystic fibrosis
Hereditary combined deficiency of vitamin K-dependent clotting factors
Laron syndrome
Multiple endocrine neoplasia type 1
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Short stature due to partial GHR deficiency
Congenital alpha2 antiplasmin deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
FGA P02671134820
FGB P02675134830
FGG P02679134850
Very frequent
- Autosomal dominant inheritance
- Epistaxis / nose bleeding
- Gastrointestinal bleeding / hemorrhage / hematemesis / melena / rectorrhagia
- Gingivorrhagia / gingival bleeding
- Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding

Frequent
- Venous thrombosis / phlebitis / thrombophlebitis