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East Texas bleeding disorder
1 OMIM reference -
1 associated gene
13 connected diseases
No signs/symptoms info
Disease Type of connection
Cerebral sinovenous thrombosis
Budd-Chiari syndrome
Congenital factor V deficiency
Congenital factor II deficiency
Hereditary thrombophilia due to congenital protein S deficiency
Congenital factor X deficiency
Essential thrombocythemia
Myelofibrosis with myeloid metaplasia
B-cell chronic lymphocytic leukemia
Hereditary thrombophilia due to congenital protein C deficiency
Alpha-1-antichymotrypsin deficiency
Autosomal dominant severe congenital neutropenia
Cyclic neutropenia
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: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
F5 P12259612309
No signs/symptoms info available.