Human Gene Set: HP_BLINDNESS


Standard name HP_BLINDNESS
Systematic name M34841
Brief description Blindness
Full description or abstract Blindness is the condition of lacking visual perception defined as visual perception below 3/60 and/or a visual field of no greater than 10 degrees in radius around central fixation. [https://orcid.org/0000-0001-8727-6592, PMID:28779882]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0000618
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0000618
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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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Show members (show 277 source identifiers mapped to 277 genes)
Version history 2023.1.Hs: Updated to HPO Release 2023-01-27.

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