Human Phenotype Ontology 
Grandparent Node:
expandVisual field defect (HP:0001123)help
Parent Node:
expandAbnormal visual field test (HP:0030588)help
..Starting node
..expandAbnormal static perimetry test (HP:0030592)help
Term ID: 30592
Name: Abnormal static perimetry test
Synonym:
Definition:
Comments:
Reference: HP:0030592
Genes and Diseases:
 
       Child Nodes:
........expandAbnormal static automated perimetry test (HP:0030595) help
................... HP:0030596 Abnormal Humphrey SITA 30-2 perimetry test
................... HP:0030597 Abnormal Humphrey SITA 24-2 perimetry test
................... HP:0030598 Abnormal Humphrey SITA 10-2 perimetry test
................... HP:0030599 Abnormal Estermann grid perimetry test

 Sister Nodes: 
..expandAbnormal Amsler grid test (HP:0030590) help
..expandAbnormal confrontational visual field test (HP:0030589) help
..expandAbnormal kinetic perimetry test (HP:0030591) 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:0030592HP:0030592Abnormal static perimetry test0 CL E G H
HP:0030592HP:0030595Abnormal static automated perimetry test1 CL E G H
HP:0030592HP:0030598Abnormal Humphrey SITA 10-2 perimetry test2 CL E G H
HP:0030592HP:0030597Abnormal Humphrey SITA 24-2 perimetry test2 CL E G H
HP:0030592HP:0030596Abnormal Humphrey SITA 30-2 perimetry test2 CL E G H
HP:0030592HP:0030599Abnormal Estermann grid perimetry test2 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.