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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Craniopharyngioma
Familial advanced sleep-phase syndrome

BRAF CSNK1D
CTNNB1 PER2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.62)
CSNK1D



Citations in the biomedical literature:


Craniopharyngioma
BRAF CTNNB1
Familial advanced sleep-phase syndrome
CSNK1D PER2



Craniopharyngioma
Familial advanced sleep-phase syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- FASPS

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: -
Average age onset: childhood
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.