Nominal Aphasia

Alias:
Anomia
Anomic Aphasia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Nominal Aphasia, also known as anomia, is related to frontotemporal lobar degeneration with tdp43 inclusions, grn-related and semantic dementia, and has symptoms including scanning speech and other symbolic dysfunction. An important gene associated with Nominal Aphasia is CBS (Cystathionine Beta-Synthase), and among its related pathways/superpathways are Alzheimer's disease and miRNA effects and Neuroscience. The drugs Sulfamethazine and Cefpodoxime have been mentioned in the context of this disorder. Affiliated tissues include brain and temporal lobe, and related phenotypes are nervous system and homeostasis/metabolism
Related ID:
MESH:D000849

Basic Information

Inheritance
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Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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15
319
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Medical Symptom

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Gene & Mutation

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References Literature

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