Human Phenotype Ontology 
Grandparent Node:
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Visual field defect (HP:0001123)help
Parent Node:
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Constriction of peripheral visual field (HP:0001133)help
..Starting node
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Mild constriction of peripheral visual field (HP:0030522)help
Term ID: 30522
Name: Mild constriction of peripheral visual field
Synonym: Mild peripheral visual field loss
Definition: A diminution of the peripheral visual field whereby at least 50 degrees of central field are preserved in all meridians.
Comments:
Reference: HP:0030522
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandModerate constriction of peripheral visual field (HP:0030525) help
..expandobsolete Peripheral visual field constriction with 30-39 degrees central field preserved (HP:0030524) help
..expandobsolete Peripheral visual field constriction with 40-50 degrees central field preserved (HP:0030523) help
..expandPeripheral visual field loss (HP:0007994) help
..expandSevere constriction of peripheral visual field (HP:0030526) help
..expandVery severe constriction of peripheral visual field (HP:0030527) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030522HP:0030522Mild constriction of peripheral visual field0 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 December 15 2022 release.