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Nervous System Diseases > Neurodegenerative Diseases > Prion Diseases > Insomnia, Fatal Familial
Nervous System Diseases > Central Nervous System Diseases > Central Nervous System Infections > Prion Diseases > Insomnia, Fatal Familial
Infections > Central Nervous System Infections > Prion Diseases > Insomnia, Fatal Familial
... > Mental Disorders > Sleep Wake Disorders > Dyssomnias > Sleep Disorders, Intrinsic > Sleep Initiation and Maintenance Disorders > Insomnia, Fatal Familial
... > Nervous System Diseases > Neurologic Manifestations > Sleep Wake Disorders > Dyssomnias > Sleep Disorders, Intrinsic > Sleep Initiation and Maintenance Disorders > Insomnia, Fatal Familial
... > Pathological Conditions, Signs and Symptoms > Signs and Symptoms > Neurologic Manifestations > Sleep Wake Disorders > Dyssomnias > Sleep Disorders, Intrinsic > Sleep Initiation and Maintenance Disorders > Insomnia, Fatal Familial

Término preferido

Insomnia, Fatal Familial  

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Tipo

  • mesh:Descriptor

Definición

  • An autosomal dominant disorder characterized by degeneration of the THALAMUS and progressive insomnia. It is caused by a mutation in the prion protein (PRIONS).

Concepto genérico

Etiquetas alternativas

  • Familial Fatal Insomnia
  • Fatal Familial Insomnia
  • Insomnia Familial Fatal

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-QNF735KF-7

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RDF/XML TURTLE JSON-LD Creado 3/7/02, última modificación 17/6/19