Ideomotor Apraxia

Alias:
Apraxia, Ideomotor
Transcortical Apraxia
Limb-Kinetic Apraxia
Ideomotor Dyspraxia
Classic Apraxia
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Basic Information
Medical Symptom
Gene & Mutation
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References Literature
Ideomotor Apraxia, also known as apraxia, ideomotor, is related to apraxia and frontotemporal lobar degeneration with tdp43 inclusions, grn-related, and has symptoms including other symbolic dysfunction An important gene associated with Ideomotor Apraxia is CBS (Cystathionine Beta-Synthase), and among its related pathways/superpathways are Alzheimer's disease and miRNA effects and Presenilin-Mediated Signaling. Affiliated tissues include parietal lobe and cortex, and related phenotypes are nervous system and homeostasis/metabolism
Related ID:
MESH:D020240

Basic Information

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Reference
MALACARDS
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Unknown
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14
358
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Medical Symptom

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Gene & Mutation

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References Literature

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