Huntington Disease-Like 1 (HDL1)

Alias:

Hdl1

Early-Onset Prion Disease with Prominent Psychiatric Features

Huntington-Like Neurodegenerative Disorder 1

Huntington's Disease-Like 1

Hln1

Prion Disease, Early-Onset, with Prominent Psychiatric Features

Huntington-Like Neurodegenerative Disorder, Autosomal Dominant

Autosomal Dominant Huntington-Like Neurodegenerative Disorder

Huntington Disease-Like, Type 1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Huntington Disease-Like 1, also known as hdl1, is related to huntington disease-like 2 and huntington's disease-like syndrome, and has symptoms including ataxia, muscle rigidity and grimacing. An important gene associated with Huntington Disease-Like 1 is PRNP (Prion Protein (Kanno Blood Group)), and among its related pathways/superpathways is Prion disease pathway. Affiliated tissues include eye and cortex, and related phenotypes are chorea and depression

Related ID：

MALACARDS：HNT010

OMIM：603218