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Craniopharyngioma
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Atypical Werner syndrome
1 associated gene
No signs/symptoms info
Craniopharyngioma
Atypical Werner syndrome

BRAF
(UniProt - OMIM)
 LMNA
(UniProt - OMIM)
CTNNB1
(UniProt - OMIM)

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


Citations in the biomedical literature:


Craniopharyngioma
BRAF CTNNB1
Atypical Werner syndrome
LMNA



Craniopharyngioma
Atypical Werner syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Atypical progeroid syndrome
Classification (Orphanet):
- Rare endocrine disease
- Rare neurologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: D003397
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.