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CLN2 disease
1 OMIM reference -
1 associated gene
12 connected diseases
No signs/symptoms info
Disease Type of connection
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
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):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: -
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.