Human Gene Set: HP_AGNOSIA


Standard name HP_AGNOSIA
Systematic name M37563
Brief description Agnosia
Full description or abstract Inability to recognize objects not because of sensory deficit but because of the inability to combine components of sensory impressions into a complete pattern. Thus, agnosia is a neurological condition which results in an inability to know, to name, to identify, and to extract meaning from visual, auditory, or tactile impressions. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0010524
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0010524
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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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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
Advanced query Further investigate these 31 genes
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Show members (show 31 source identifiers mapped to 31 genes)
Version history 2023.1.Hs: Updated to HPO Release 2023-01-27.

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