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Spinocerebellar ataxia type 19/22
1 OMIM reference -
1 associated gene
13 connected diseases
No signs/symptoms info
Disease Type of connection
Brugada syndrome
Desmoplastic small round cell tumor
Ewing sarcoma
Extraskeletal Ewing sarcoma
Extraskeletal myxoid chondrosarcoma
Greenberg dysplasia
Isolated CoQ-cytochrome C reductase deficiency
Isolated NADH-CoQ reductase deficiency
Melanoma of soft part
Proximal myotonic myopathy
Reynolds syndrome
Translocation renal cell carcinoma
X-linked Emery-Dreifuss muscular dystrophy
Synonym(s):
- SCA19/22
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: C537198
Gene symbol UniProt reference OMIM reference
KCND3 Q9UK17605411
No signs/symptoms info available.