Human Gene Set: HP_HYPERMETROPIA


Standard name HP_HYPERMETROPIA
Systematic name M34786
Brief description Hypermetropia
Full description or abstract An abnormality of refraction characterized by the ability to see objects in the distance clearly, while objects nearby appear blurry. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0000540
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0000540
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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 284 genes
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Show members (show 285 source identifiers mapped to 284 genes)
Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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