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Fetal and neonatal alloimmune thrombocytopenia
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital factor XI deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Fetal and neonatal alloimmune thrombocytopenia
Congenital factor XI deficiency

CD109
(UniProt - OMIM)
 F11
(UniProt - OMIM)
GP1BA
(UniProt - OMIM)
GP1BB
(UniProt - OMIM)
ITGA2
(UniProt - OMIM)
ITGA2B
(UniProt - OMIM)
ITGB3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GP1BA
(0.75)
F11


Citations in the biomedical literature:


Fetal and neonatal alloimmune thrombocytopenia
CD109 GP1BA GP1BB ITGA2 ITGA2B ITGB3

Congenital factor XI deficiency
F11



Fetal and neonatal alloimmune thrombocytopenia
Congenital factor XI deficiency

Synonym(s):
- NAIT
Synonym(s):
- Hemophilia C
- PTA deficiency
- Plasma thromboplastin antecedent deficiency
- Rosenthal factor deficiency
- Rosenthal syndrome
Classification (Orphanet):
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
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:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.