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Craniopharyngioma
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive axonal neuropathy with neuromyotonia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Craniopharyngioma
Autosomal recessive axonal neuropathy with neuromyotonia

BRAF
(UniProt - OMIM)
 HINT1
(UniProt - OMIM)
CTNNB1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CTNNB1
(0.82)
HINT1


Citations in the biomedical literature:


Craniopharyngioma
BRAF CTNNB1
Autosomal recessive axonal neuropathy with neuromyotonia
HINT1



Craniopharyngioma
Autosomal recessive axonal neuropathy with neuromyotonia

Synonym(s):
(no synonyms)

Synonym(s):
- ARAN-NM
- ARCMT2-NM
- Autosomal recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia
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: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
1 MeSH reference: D003397
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.