Human Gene Set: HP_MYOPIA


Standard name HP_MYOPIA
Systematic name M34790
Brief description Myopia
Full description or abstract An abnormality of refraction characterized by the ability to see objects nearby clearly, while objects in the distance appear blurry. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0000545
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0000545
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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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