Human Phenotype Ontology 
Grandparent Node:
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Abnormality of vision (HP:0000504)help
Parent Node:
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Visual field defect (HP:0001123)help
..Starting node
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Abnormal visual field test (HP:0030588)help
Term ID: 30588
Name: Abnormal visual field test
Synonym:
Definition: Abnormal result of a test designed to test an individual's central and peripheral vision by determining the ability of the individual to perceive objects at differing locations of the visual field.
Comments:
Reference: HP:0030588
Genes and Diseases:
 
       Child Nodes:
........expandAbnormal confrontational visual field test (HP:0030589) help
........expandAbnormal Amsler grid test (HP:0030590) help
........expandAbnormal kinetic perimetry test (HP:0030591) help
................... HP:0030593 Abnormal manual kinetic perimetry test
................... HP:0030594 Abnormal automated kinetic perimetry test
........expandAbnormal static perimetry test (HP:0030592) help
................... HP:0030595 Abnormal static automated perimetry test

 Sister Nodes: 
..expandAltitudinal visual field defect (HP:0030531) help
..expandBlind-spot enlargment (HP:0030644) help
..expandConstriction of peripheral visual field (HP:0001133) help
..expandGlaucomatous visual field defect (HP:0007854) help
..expandHemianopia (HP:0012377) help
..expandLarge central visual field defect (HP:0001129) help
..expandProgressive visual field defects (HP:0007987) help
..expandScotoma (HP:0000575) 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:0030588HP:0030588Abnormal visual field test0AKT1 CL E G H207391ORPHA:2495Meningioma54
HP:0030588HP:0030588Abnormal visual field test0ATP6 CL E G H45087414ORPHA:644NARP syndromeHP:0040282 - Frequent
HP:0030588HP:0030588Abnormal visual field test0BAP1 CL E G H8314950ORPHA:2495Meningioma184
HP:0030588HP:0030588Abnormal visual field test0BRAF CL E G H6731097ORPHA:54595CraniopharyngiomaHP:0040282 - Frequent276
HP:0030588HP:0030588Abnormal visual field test0CDH23 CL E G H6407213733ORPHA:91347TSH-secreting pituitary adenomaHP:0040283 - Occasional636
HP:0030588HP:0030588Abnormal visual field test0CTNNB1 CL E G H14992514ORPHA:54595CraniopharyngiomaHP:0040282 - Frequent88
HP:0030588HP:0030588Abnormal visual field test0NF2 CL E G H47717773ORPHA:2495Meningioma220
HP:0030588HP:0030588Abnormal visual field test0PDGFB CL E G H51558800ORPHA:2495Meningioma9
HP:0030588HP:0030588Abnormal visual field test0PIK3CA CL E G H52908975ORPHA:2495Meningioma162
HP:0030588HP:0030588Abnormal visual field test0SMARCB1 CL E G H659811103ORPHA:2495Meningioma87
HP:0030588HP:0030588Abnormal visual field test0SMARCE1 CL E G H660511109ORPHA:2495Meningioma47
HP:0030588HP:0030588Abnormal visual field test0SMO CL E G H660811119ORPHA:2495Meningioma22
HP:0030588HP:0030588Abnormal visual field test0SUFU CL E G H5168416466ORPHA:2495Meningioma124
HP:0030588HP:0030588Abnormal visual field test0TERT CL E G H701511730ORPHA:2495Meningioma238
HP:0030588HP:0030588Abnormal visual field test0TRAF7 CL E G H8423120456ORPHA:2495Meningioma
HP:0030588HP:0030592Abnormal static perimetry test1 CL E G H
HP:0030588HP:0030590Abnormal Amsler grid test1 CL E G H
HP:0030588HP:0030589Abnormal confrontational visual field test1 CL E G H
HP:0030588HP:0030591Abnormal kinetic perimetry test1AKT1 CL E G H207391ORPHA:2495MeningiomaHP:0040283 - Occasional54
HP:0030588HP:0030591Abnormal kinetic perimetry test1BAP1 CL E G H8314950ORPHA:2495MeningiomaHP:0040283 - Occasional184
HP:0030588HP:0030591Abnormal kinetic perimetry test1NF2 CL E G H47717773ORPHA:2495MeningiomaHP:0040283 - Occasional220
HP:0030588HP:0030591Abnormal kinetic perimetry test1PDGFB CL E G H51558800ORPHA:2495MeningiomaHP:0040283 - Occasional9
HP:0030588HP:0030591Abnormal kinetic perimetry test1PIK3CA CL E G H52908975ORPHA:2495MeningiomaHP:0040283 - Occasional162
HP:0030588HP:0030591Abnormal kinetic perimetry test1SMARCB1 CL E G H659811103ORPHA:2495MeningiomaHP:0040283 - Occasional87
HP:0030588HP:0030591Abnormal kinetic perimetry test1SMARCE1 CL E G H660511109ORPHA:2495MeningiomaHP:0040283 - Occasional47
HP:0030588HP:0030591Abnormal kinetic perimetry test1SMO CL E G H660811119ORPHA:2495MeningiomaHP:0040283 - Occasional22
HP:0030588HP:0030591Abnormal kinetic perimetry test1SUFU CL E G H5168416466ORPHA:2495MeningiomaHP:0040283 - Occasional124
HP:0030588HP:0030591Abnormal kinetic perimetry test1TERT CL E G H701511730ORPHA:2495MeningiomaHP:0040283 - Occasional238
HP:0030588HP:0030591Abnormal kinetic perimetry test1TRAF7 CL E G H8423120456ORPHA:2495MeningiomaHP:0040283 - Occasional
HP:0030588HP:0030595Abnormal static automated perimetry test2 CL E G H
HP:0030588HP:0030594Abnormal automated kinetic perimetry test2 CL E G H
HP:0030588HP:0030593Abnormal manual kinetic perimetry test2 CL E G H
HP:0030588HP:0030599Abnormal Estermann grid perimetry test3 CL E G H
HP:0030588HP:0030598Abnormal Humphrey SITA 10-2 perimetry test3 CL E G H
HP:0030588HP:0030597Abnormal Humphrey SITA 24-2 perimetry test3 CL E G H
HP:0030588HP:0030596Abnormal Humphrey SITA 30-2 perimetry test3 CL E G H


Genes (15) :AKT1 ATP6 BAP1 BRAF CDH23 CTNNB1 NF2 PDGFB PIK3CA SMARCB1 SMARCE1 SMO SUFU TERT TRAF7

Diseases (4) :ORPHA:2495 ORPHA:644 ORPHA:54595 ORPHA:91347
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.