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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
Synonym(s):
- 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.