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GENATLAS PHENOTYPE

last update : 16/05/2008

Symbol	HDL1
Location	20p13
Name	Huntington-like 1
Other name(s)	Huntington-like neurodegeneratice disorder 1
Corresponding gene	PRNP
Other symbol(s)	HLN1
Main clinical features	neurodegenerative disorder, prion disease, spongiform encephalopathy, early-onset with prominent psychiatric features, characterized by dementia, motor decline, and ataxia
Genetic determination	autosomal dominant
Related entries	including prion disease with protracted course (in Brazilian people)
Function/system disorder	neurology
	psychiatric disorder
Type	disease

Gene product

Name	prion protein

Remark(s)