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Familial infantile bilateral striatal necrosis
2 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
17q21.31 microdeletion syndrome
1 associated gene
No signs/symptoms info
Familial infantile bilateral striatal necrosis
17q21.31 microdeletion syndrome

ADAR
(UniProt - OMIM)
 KANSL1
(UniProt - OMIM)
MT-ATP6
(UniProt - OMIM)
NUP62
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NUP62
(0.63)
KANSL1


Citations in the biomedical literature:


Familial infantile bilateral striatal necrosis
ADAR MT-ATP6 NUP62
17q21.31 microdeletion syndrome
KANSL1



Familial infantile bilateral striatal necrosis
17q21.31 microdeletion syndrome

Synonym(s):
- Familial IBSN
- Familial infantile striatonigral degeneration
- Familial infantile striatonigral necrosis
Synonym(s):
- Del(17)(q21.31)
- Monosomy 17q21.31
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.