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Congenital factor XI deficiency
1 OMIM reference -
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
Congenital high-molecular-weight kininogen deficiency
Bernard-Soulier syndrome
Fetal and neonatal alloimmune thrombocytopenia
Von Willebrand disease, platelet type
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Cerebral sinovenous thrombosis
Congenital alpha2 antiplasmin deficiency
Congenital factor II deficiency
- Hemophilia C
- PTA deficiency
- Plasma thromboplastin antecedent deficiency
- Rosenthal factor deficiency
- Rosenthal syndrome

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: 1-9 / 1 000 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
F11 P03951264900
No signs/symptoms info available.