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CLN8 disease
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Pelizaeus-Merzbacher disease, transitional form
1 associated gene
No signs/symptoms info
CLN8 disease
Pelizaeus-Merzbacher disease, transitional form

CLN8
(UniProt - OMIM)
 PLP1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CLN8
(0.63)
PLP1


Citations in the biomedical literature:


CLN8 disease
CLN8
Pelizaeus-Merzbacher disease, transitional form
PLP1



CLN8 disease
Pelizaeus-Merzbacher disease, transitional form

Synonym(s):
(no synonyms)

Synonym(s):
- Transitional PMD
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):
- Endocrine, nutritional and metabolic diseases -
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: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.