Human Phenotype Ontology 
Grandparent Node:
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Color vision defect (HP:0000551)help
Parent Node:
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Dyschromatopsia (HP:0007641)help
..Starting node
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Anomalous trichromacy (HP:0011519)help
Term ID: 11519
Name: Anomalous trichromacy
Synonym:
Definition: Individuals with anomalous trichromacy possess three types of cones, but one of the three types of cones has an abnormal spectral sensitivity compared to normal cones.
Comments:
Reference: HP:0011519
Genes and Diseases:
 
       Child Nodes:
........expandTritanomaly (HP:0000552) help
........expandDeuteranomaly (HP:0011520) help
........expandProtanomaly (HP:0200018) help

 Sister Nodes: 
..expandDichromacy (HP:0011518) help
..expandRed-green dyschromatopsia (HP:0000642) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011519HP:0011519Anomalous trichromacy0 CL E G H
HP:0011519HP:0000552Tritanomaly1 CL E G H
HP:0011519HP:0200018Protanomaly1 CL E G H
HP:0011519HP:0011520Deuteranomaly1 CL E G H


Genes (7) :DNM1L NR2E3 OPA1 OPA3 OPN1LW OPN1MW OPN1SW

Diseases (8) :610708 611131 125250 165500 67036 303900 303800 190900
 

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