Cytoscape Web
Click node...

Craniopharyngioma
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial infantile bilateral striatal necrosis
2 OMIM references -
3 associated genes
No signs/symptoms info
Craniopharyngioma
Familial infantile bilateral striatal necrosis

BRAF
(UniProt - OMIM)
 ADAR
(UniProt - OMIM)
CTNNB1
(UniProt - OMIM)
 MT-ATP6
(UniProt - OMIM)
NUP62
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CTNNB1
(0.63)
NUP62


Citations in the biomedical literature:


Craniopharyngioma
BRAF CTNNB1
Familial infantile bilateral striatal necrosis
ADAR MT-ATP6 NUP62



Craniopharyngioma
Familial infantile bilateral striatal necrosis

Synonym(s):
(no synonyms)

Synonym(s):
- Familial IBSN
- Familial infantile striatonigral degeneration
- Familial infantile striatonigral necrosis
Classification (Orphanet):
- Rare endocrine disease
- Rare neurologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
1 MeSH reference: D003397
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.