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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Pelizaeus-Merzbacher disease, connatal form
Juvenile Huntington disease

PLP1 HTT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PLP1
(0.68)
HTT



Citations in the biomedical literature:


Pelizaeus-Merzbacher disease, connatal form
PLP1
Juvenile Huntington disease
HTT



Pelizaeus-Merzbacher disease, connatal form
Juvenile Huntington disease

Synonym(s):
- Connatal PMD
- Pelizaeus-Merzbacher disease type II
- Severe PMD

Synonym(s):
- JHD
- Juvenile Huntington chorea

Classification (Orphanet):
- 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: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: x-linked recessive
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.