Human Gene Set: HP_AMBLYOPIA


Standard name HP_AMBLYOPIA
Systematic name M34858
Brief description Amblyopia
Full description or abstract Reduced visual acuity that is uncorrectable by lenses in the absence of detectable anatomic defects in the eye or visual pathways. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0000646
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0000646
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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 117 genes
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Show members (show 117 source identifiers mapped to 117 genes)
Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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