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Craniopharyngioma
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant secondary polycythemia
2 OMIM references -
2 associated genes
No signs/symptoms info
Craniopharyngioma
Autosomal dominant secondary polycythemia

BRAF
(UniProt - OMIM)
 EGLN1
(UniProt - OMIM)
CTNNB1
(UniProt - OMIM)
 EPAS1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CTNNB1
(0.63)
EPAS1


Citations in the biomedical literature:


Craniopharyngioma
BRAF CTNNB1
Autosomal dominant secondary polycythemia
EGLN1 EPAS1



Craniopharyngioma
Autosomal dominant secondary polycythemia

Synonym(s):
(no synonyms)

Synonym(s):
- Autosomal dominant secondary erythrocytosis
Classification (Orphanet):
- Rare endocrine disease
- Rare neurologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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: unknown
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.