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CLN8 disease
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Primary dystonia, DYT4 type
1 OMIM reference -
1 associated gene
No signs/symptoms info
CLN8 disease
Primary dystonia, DYT4 type

CLN8
(UniProt - OMIM)
 TUBB4A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CLN8
(0.63)
TUBB4A


Citations in the biomedical literature:


CLN8 disease
CLN8
Primary dystonia, DYT4 type
TUBB4A



CLN8 disease
Primary dystonia, DYT4 type

Synonym(s):
(no synonyms)

Synonym(s):
- DYT4
- Hereditary whispering dysphonia
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.