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Fetal and neonatal alloimmune thrombocytopenia
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital myopathy with excess of thin filaments
1 OMIM reference -
1 associated gene
No signs/symptoms info
Fetal and neonatal alloimmune thrombocytopenia
Congenital myopathy with excess of thin filaments

CD109
(UniProt - OMIM)
 ACTA1
(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)
ITGA2
(0.52)
ACTA1


Citations in the biomedical literature:


Fetal and neonatal alloimmune thrombocytopenia
CD109 GP1BA GP1BB ITGA2 ITGA2B ITGB3

Congenital myopathy with excess of thin filaments
ACTA1



Fetal and neonatal alloimmune thrombocytopenia
Congenital myopathy with excess of thin filaments

Synonym(s):
- NAIT
Synonym(s):
- Actin myopathy
Classification (Orphanet):
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.