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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital factor II deficiency
Atypical hemolytic uremic syndrome with thrombomodulin anomaly

F2 THBD


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
F2
(0.9)
THBD



Citations in the biomedical literature:


Congenital factor II deficiency
F2
Atypical hemolytic uremic syndrome with thrombomodulin anomaly
THBD



Congenital factor II deficiency
Atypical hemolytic uremic syndrome with thrombomodulin anomaly

Synonym(s):
- Dysprothrombinemia
- Hypoprothrombinemia
- Prothrombin deficiency

Synonym(s):
- Atypical HUS with thrombomodulin anomaly
- D-HUS with thrombomodulin anomaly
- Hemolytic-uremic syndrome without diarrhea with thrombomodulin anomaly
- aHUS with thrombomodulin anomaly

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare renal disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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: variable
Average age of death: any age
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.