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Fetal and neonatal alloimmune thrombocytopenia
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant rhegmatogenous retinal detachment
1 OMIM reference -
1 associated gene
No signs/symptoms info
Fetal and neonatal alloimmune thrombocytopenia
Autosomal dominant rhegmatogenous retinal detachment

CD109
(UniProt - OMIM)
 COL2A1
(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)
ITGA2B
(0.85)
COL2A1


Citations in the biomedical literature:


Fetal and neonatal alloimmune thrombocytopenia
CD109 GP1BA GP1BB ITGA2 ITGA2B ITGB3

Autosomal dominant rhegmatogenous retinal detachment
COL2A1



Fetal and neonatal alloimmune thrombocytopenia
Autosomal dominant rhegmatogenous retinal detachment

Synonym(s):
- NAIT
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare hematologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
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.