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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 associated genes
No signs/symptoms info
Congenital factor II deficiency
Pediatric systemic lupus erythematosus

F2 IRAK1
PTPN22
SPP1
STAT4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
F2
(0.52)
SPP1



Citations in the biomedical literature:


Congenital factor II deficiency
F2
Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4



Congenital factor II deficiency
Pediatric systemic lupus erythematosus

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

Synonym(s):
- SLE, pediatric onset

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare neurologic disease
- Rare renal disease
- Rare respiratory disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -

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:
(no data available)

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

No signs/symptoms info available.