Human Phenotype Ontology 
Grandparent Node:
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Dyschromatopsia (HP:0007641)help
Parent Node:
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Anomalous trichromacy (HP:0011519)help
Parent Node:
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Red-green dyschromatopsia (HP:0000642)help
..Starting node
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Deuteranomaly (HP:0011520)help
Term ID: 11520
Name: Deuteranomaly
Synonym: Deuteranomoly; Green-weak
Definition: A type of anomalous trichromacy associated with abnormal M photopigment, such that the absorption spectrum is shifted toward L wavelengths. Affected individuals have difficulties distinguishing between red and green.
Comments:
Reference: HP:0011520
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDeuteranopia (HP:0011521) help
..expandProtanomaly (HP:0200018) help
..expandProtanopia (HP:0011522) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0011520HP:0011520Deuteranomaly0OPN1MW CL E G H2652303800Deuteranopia303800C0155016OMIM12604206300821
HP:0011520HP:0011520Deuteranomaly0OPN1MW CL E G H2652303800Deuteranopia303800C0155016OMIM12554206300821
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :OPN1MW

Diseases (1) :303800
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.