ODCs

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

PROTEIN INTERACTIONS: 1

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

Huntington disease-like 1

Autosomal dominant spastic paraplegia type 13


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PRNP	(0.66)	HSPD1

Citations in the biomedical literature:

Huntington disease-like 1		Autosomal dominant spastic paraplegia type 13
	Synonym(s): - Early onset prion disease with prominent psychiatric features - HDL1		Synonym(s): - SPG13

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537485

No signs/symptoms info available.