Human Phenotype Ontology 
Grandparent Node:
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Retinopathy (HP:0000488)help
Parent Node:
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Retinopathy of prematurity (HP:0500049)help
..Starting node
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Retinopathy of prematurity plus (HP:0500062)help
Term ID: 500062
Name: Retinopathy of prematurity plus
Synonym: ROP plus
Definition: Venous dilatation and arteriolar tortuosity of the posterior retinal vessels and may later increase in severity to include iris vascular engorgement, poor pupillary dilatation (rigid pupil), and vitreous haze. This definition has been further refined in the later clinical trials in which the diagnosis of plus disease could be made if sufficient vascular dilatation and tortuosity are present in at least 2 quadrants of the eye.
Comments:
Reference: HP:0500062
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandRetinopathy of prematurity pre-plus (HP:0500063) help
..expandRetinopathy of prematurity prethreshold (HP:0500065) help
..expandRetinopathy of prematurity stage 1 (HP:0500050) help
..expandRetinopathy of prematurity stage 2 (HP:0500051) help
..expandRetinopathy of prematurity stage 3 (HP:0500052) help
..expandRetinopathy of prematurity stage 4 (HP:0500053) help
..expandRetinopathy of prematurity stage 5 (HP:0500056) help
..expandRetinopathy of prematurity threshold (HP:0500064) help
..expandRetinopathy of prematurity zone I (HP:0500059) help
..expandRetinopathy of prematurity zone II (HP:0500060) help
..expandRetinopathy of prematurity zone III (HP:0500061) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500062HP:0500062Retinopathy of prematurity plus0 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 August 2021 release.