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Spinocerebellar ataxia type 18
1 OMIM reference -
1 associated gene
22 connected diseases
No signs/symptoms info
Disease Type of connection
5q14.3 microdeletion syndrome
Adrenocortical carcinoma
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Autosomal dominant nonsyndromic intellectual deficit
B-cell chronic lymphocytic leukemia
Boomerang dysplasia
Craniopharyngioma
Desmoid tumor
Essential thrombocythemia
Familial pancreatic carcinoma
Giant cell glioblastoma
Gliosarcoma
Hepatocellular carcinoma, childhood-onset
Li-Fraumeni syndrome
Noonan syndrome
Papilloma of choroid plexus
Pilomatrixoma
Precursor B-cell acute lymphoblastic leukemia
Spondylocarpotarsal synostosis
2q37 microdeletion syndrome
Synonym(s):
- SCA18
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
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: C537197
Gene symbol UniProt reference OMIM reference
IFRD1 O00458603502
No signs/symptoms info available.