Human Gene Set: HP_HAND_APRAXIA


Standard name HP_HAND_APRAXIA
Systematic name M41569
Brief description Hand apraxia
Full description or abstract Inability to perform purposeful (learned) movements with the hand upon command, even though the command is understood and there is a willingness to perform the movement. Hand apraxia includes the inability to grasp, pick up, and hold large and small objects. [PMID:20345957]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0032588
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0032588
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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 2024.1.Hs: Updated to HPO Release 2024-04-26.

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