Human Gene Set: HP_CEREBRAL_VISUAL_IMPAIRMENT


Standard name HP_CEREBRAL_VISUAL_IMPAIRMENT
Systematic name M38805
Brief description Cerebral visual impairment
Full description or abstract A form of loss of vision caused by damage to the visual cortex rather than a defect in the eye. [https://orcid.org/0000-0002-0736-9199, PMID:28082927]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0100704
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0100704
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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 2023.1.Hs: Updated to HPO Release 2023-01-27.

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