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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
aphasia +     
amyotrophic lateral sclerosis type 15  
amyotrophic lateral sclerosis type 22  
amyotrophic lateral sclerosis type 6  
Broca Aphasia 
Conduction Aphasia 
corticobasal degeneration syndrome 
Familial Developmental Dysphasia 
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis +   
GRN-related frontotemporal lobar degeneration with TDP43 inclusions  
inclusion body myopathy with Paget disease of bone and frontotemporal dementia +   
nominal aphasia 
Pallidopontonigral Degeneration 
Pick's disease  
primary progressive aphasia +   
A frontotemporal dementia that characterized by the progressive onset of language impairments, and gradual deterioration of these abilities over time, associated with atrophy of the language network of the brain, including frontal, temporal, and parietal regions of the left hemisphere. It is caused by a loss of tissue (atrophy) in the area of the brain that is responsible for producing language. (DO)
Wernicke Aphasia 

Synonyms
Exact Synonyms: Mesulam Syndrome ;   Mesulam's Syndrome ;   Primary Progressive Aphasias
Related Synonyms: Primary Progressive Aphasia, Susceptibility To
Primary IDs: MESH:D018888
Alternate IDs: DOID:9008293
Xrefs: EFO:0009053 ;   GARD:8541 ;   ORDO:95432
Definition Sources: https://pubmed.ncbi.nlm.nih.gov/21325651/ "DO" "DO", https://pubmed.ncbi.nlm.nih.gov/29392464/ "DO" "DO", https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993834/ "DO" "DO"

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