Human Phenotype Ontology 
Grandparent Node:
expandVisual acuity test abnormality (HP:0030532)help
Parent Node:
expandAbnormal pinhole visual acuity test (HP:0030535)help
..Starting node
..expandPinhole visual acuity 0.5 LogMAR (HP:0030573)help
Term ID: 30573
Name: Pinhole visual acuity 0.5 LogMAR
Synonym:
Definition:
Comments:
Reference: HP:0030573
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPinhole visual acuity 0.1 LogMAR (HP:0030569) help
..expandPinhole visual acuity 0.2 LogMAR (HP:0030570) help
..expandPinhole visual acuity 0.3 LogMAR (HP:0030571) help
..expandPinhole visual acuity 0.4 LogMAR (HP:0030572) help
..expandPinhole visual acuity 0.6 LogMAR (HP:0030574) help
..expandPinhole visual acuity 0.7 LogMAR (HP:0030575) help
..expandPinhole visual acuity 0.8 LogMAR (HP:0030576) help
..expandPinhole visual acuity 0.9 LogMAR (HP:0030577) help
..expandPinhole visual acuity 1.0 LogMAR (HP:0030578) help
..expandPinhole visual acuity 1.1 LogMAR (HP:0030579) help
..expandPinhole visual acuity 1.2 LogMAR (HP:0030580) help
..expandPinhole visual acuity 1.3 LogMAR (HP:0030581) help
..expandPinhole visual acuity 2.0 LogMAR (HP:0030582) help
..expandPinhole visual acuity 3.0 LogMAR (HP:0030583) 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:0030573HP:0030573Pinhole visual acuity 0.5 LogMAR0 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.