Human Gene Set: HP_DYSCHROMATOPSIA


Standard name HP_DYSCHROMATOPSIA
Systematic name M37103
Brief description Dyschromatopsia
Full description or abstract A form of colorblindness in which only two of the three fundamental colors can be distinguished due to a lack of one of the retinal cone pigments. [HPO_CONTRIBUTOR:DDD_ncarter]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0007641
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0007641
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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 34 genes
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Show members (show 34 source identifiers mapped to 34 genes)
Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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