Human Gene Set: HP_OROMOTOR_APRAXIA


Standard name HP_OROMOTOR_APRAXIA
Systematic name M37031
Brief description Oromotor apraxia
Full description or abstract Oral-motor apraxia is the inability to volitionally sequence oral movements of the speech structure for nonspeech tasks in the absence of neuromuscular deficits such as paralysis or muscle weakness. Oral-motor apraxia is diagnosed when, despite intact sensory motor function an individual is unable to use these effector systems under voluntary control. [PMID:26275812]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0007301
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0007301
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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