ODCs

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

COMMON GENES: 1

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

Huntington disease-like 1

Gerstmann-Straussler-Scheinker syndrome

PRNP

Citations in the biomedical literature:

Huntington disease-like 1		Gerstmann-Straussler-Scheinker syndrome
	Synonym(s): - Early onset prion disease with prominent psychiatric features - HDL1		Synonym(s): - Subacute spongiform encephalopathy, Gerstmann-Straussler type

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Certain infectious and parasitic diseases -

	Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood 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: D016098

No signs/symptoms info available.