Human Gene Set: HP_OCULOMOTOR_APRAXIA


Standard name HP_OCULOMOTOR_APRAXIA
Systematic name M34866
Brief description Oculomotor apraxia
Full description or abstract Ocular motor apraxia is a deficiency in voluntary, horizontal, lateral, fast eye movements (saccades) with retention of slow pursuit movements. The inability to follow objects visually is often compensated by head movements. There may be decreased smooth pursuit, and cancelation of the vestibulo-ocular reflex. [https://orcid.org/0000-0002-0736-9199, PMID:20615230]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0000657
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0000657
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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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