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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Pilomatrixoma
Spinocerebellar ataxia type 18

CTNNB1 IFRD1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.63)
IFRD1



Citations in the biomedical literature:


Pilomatrixoma
CTNNB1
Spinocerebellar ataxia type 18
IFRD1



Pilomatrixoma
Spinocerebellar ataxia type 18

Synonym(s):
- Epithelioma calcificans of Malherbe
- Pilomatricoma

Synonym(s):
- SCA18

Classification (Orphanet):
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D018296
External references:
1 OMIM reference -
1 MeSH reference: C537197

No signs/symptoms info available.