Human Gene Set: HP_ABNORMAL_CENTRAL_SENSORY_FUNCTION


Standard name HP_ABNORMAL_CENTRAL_SENSORY_FUNCTION
Systematic name M37907
Brief description Abnormal central sensory function
Full description or abstract An abnormality of sensation related to CNS function. Assuming the primary sensory modalities are intact and the patient is alert and cooperative, the presence of an abnormality of sensory function may indicate a lesion of a parietal cortex, the thalamocortical projections to the parietal cortex, or the spinal cord. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0011730
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0011730
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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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