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Distal 17p13.3 microdeletion syndrome
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Fetal and neonatal alloimmune thrombocytopenia
6 associated genes
No signs/symptoms info
Distal 17p13.3 microdeletion syndrome
Fetal and neonatal alloimmune thrombocytopenia

YWHAE
(UniProt - OMIM)
 CD109
(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)
YWHAE
(0.63)
GP1BA


Citations in the biomedical literature:


Distal 17p13.3 microdeletion syndrome
YWHAE
Fetal and neonatal alloimmune thrombocytopenia
CD109 GP1BA GP1BB ITGA2 ITGA2B ITGB3



Distal 17p13.3 microdeletion syndrome
Fetal and neonatal alloimmune thrombocytopenia

Synonym(s):
- Distal del(17)(p13.3 )
- Distal monosomy 17p13.3
Synonym(s):
- NAIT
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare hematologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.