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Congenital factor X deficiency
1 OMIM reference -
1 associated gene
15 connected diseases
No signs/symptoms info
Disease Type of connection
Mild hemophilia A
Moderately severe hemophilia A
Severe hemophilia A
Symptomatic form of hemophilia A in female carriers
Budd-Chiari syndrome
Cerebral sinovenous thrombosis
Congenital factor V deficiency
East Texas bleeding disorder
Hypoplasminogenemia
Ligneous conjunctivitis
Congenital factor VII deficiency
Hereditary thrombophilia due to congenital protein S deficiency
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
Hereditary combined deficiency of vitamin K-dependent clotting factors
Synonym(s):
- Congenital Stuart factor deficiency
- Stuart-Prower factor deficiency
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: any age
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
F10 P00742613872
No signs/symptoms info available.