Related MeSH Hierarchy (4)
Diseases [C] » Infections [C01] » Central Nervous System Infections » Prion Diseases » Insomnia, Fatal Familial
Diseases [C] » Nervous System Diseases [C10] » Central Nervous System Diseases » Central Nervous System Infections » Prion Diseases » Insomnia, Fatal Familial
Diseases [C] » Nervous System Diseases [C10] » Neurodegenerative Diseases » Prion Diseases » Insomnia, Fatal Familial
Diseases [C] » Nervous System Diseases [C10] » Sleep Wake Disorders » Dyssomnias » Sleep Disorders, Intrinsic » Sleep Initiation and Maintenance Disorders » Insomnia, Fatal Familial
Description
An autosomal dominant disorder characterized by degeneration of the THALAMUS and progressive insomnia. It is caused by a mutation in the prion protein (PRIONS). MeSH
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Phase 2 Indicated Drugs (1)
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