Human Gene Set: HP_ALEXIA


Standard name HP_ALEXIA
Systematic name M43377
Brief description Alexia
Full description or abstract An acquired type of sensory aphasia where damage to the brain leads to the loss of the ability to read. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0010523
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0010523
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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)
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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