Human Gene Set: HP_APHASIA


Standard name HP_APHASIA
Systematic name M35809
Brief description Aphasia
Full description or abstract An acquired language impairment of some or all of the abilities to produce or comprehend speech and to read or write. [PMID:27384070]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0002381
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0002381
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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 101 genes
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Show members (show 101 source identifiers mapped to 101 genes)
Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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