Human Gene Set: HP_SPEECH_APRAXIA


Standard name HP_SPEECH_APRAXIA
Systematic name M37767
Brief description Speech apraxia
Full description or abstract A type of apraxia that is characterized by difficulty or inability to execute speech movements because of problems with coordination and motor problems, leading to incorrect articulation. An increase of errors with increasing word and phrase length may occur. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0011098
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0011098
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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
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Version history 2025.1.Hs: Updated to HPO Release 2025-05-06.

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