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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Glaucomatous visual field defect (HP:0007854)help
Term ID: 7854
Name: Glaucomatous visual field defect
Synonym:
Definition:
Comments:
Reference: HP:0007854
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal visual field test (HP:0030588) help
..expandAltitudinal visual field defect (HP:0030531) help
..expandBlind-spot enlargment (HP:0030644) help
..expandConstriction of peripheral visual field (HP:0001133) 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:0007854HP:0007854Glaucomatous visual field defect0ASB10 CL E G H13637117185OMIM:603383GLAUCOMA 1, OPEN ANGLE, F; GLC1F54
HP:0007854HP:0007854Glaucomatous visual field defect0CYP1B1 CL E G H15452597ORPHA:98977Juvenile glaucomaHP:0040282 - Frequent101
HP:0007854HP:0007854Glaucomatous visual field defect0EFEMP1 CL E G H22023218ORPHA:98977Juvenile glaucomaHP:0040282 - Frequent54
HP:0007854HP:0007854Glaucomatous visual field defect0MYOC CL E G H46537610ORPHA:98977Juvenile glaucomaHP:0040282 - Frequent47


Genes (4) :ASB10 CYP1B1 EFEMP1 MYOC

Diseases (2) :OMIM:603383 ORPHA:98977
 

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