Human Phenotype Ontology 
Grandparent Node:
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Dyschromatopsia (HP:0007641)help
Parent Node:
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Dichromacy (HP:0011518)help
Parent Node:
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Red-green dyschromatopsia (HP:0000642)help
..Starting node
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Protanopia (HP:0011522)help
Term ID: 11522
Name: Protanopia
Synonym: Red-blind
Definition: Blue and green cones only; no functional red cones.
Comments:
Reference: HP:0011522
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDeuteranomaly (HP:0011520) help
..expandDeuteranopia (HP:0011521) help
..expandProtanomaly (HP:0200018) 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:0011522HP:0011522Protanopia0 CL E G H


Genes (0) :

Diseases (0) :
 

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