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Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
1 OMIM reference -
1 associated gene
12 connected diseases
No signs/symptoms info
Disease Type of connection
CLN2 disease
Precursor T-cell acute lymphoblastic leukemia
Huntington disease
Juvenile Huntington disease
Burkitt lymphoma
Giant cell glioblastoma
Gliosarcoma
Dyskeratosis congenita
Familial melanoma
Hoyeraal-Hreidarsson syndrome
Idiopathic aplastic anemia
Idiopathic pulmonary fibrosis
Synonym(s):
- Autosomal recessive spinocerebellar ataxia type 7
- SCAR7
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: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
TPP1 O14773607998
No signs/symptoms info available.