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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Juvenile Huntington disease

1 OMIM reference -
1 associated gene
No signs/symptoms info

Null syndrome

Juvenile Huntington disease

(UniProt - OMIM)

(UniProt - OMIM)


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

Citations in the biomedical literature:

Null syndrome		Juvenile Huntington disease
	Synonym(s): - PLP1 null syndrome - Pelizaeus-Merzbacher disease, null syndrome		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: unknown Average age onset: childhood Average age of death: adult 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.