Human Phenotype Ontology 
Grandparent Node:
expand
Retinopathy (HP:0000488)help
Parent Node:
expand
Retinopathy of prematurity (HP:0500049)help
..Starting node
..expand
Retinopathy of prematurity zone I (HP:0500059)help
Term ID: 500059
Name: Retinopathy of prematurity zone I
Synonym: ROP zone 1
Definition: Retinopathy which extends from the center of the optic disc to twice the distance from the center of the optic disc to the center of the macula.
Comments:
Reference: HP:0500059
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandRetinopathy of prematurity plus (HP:0500062) help
..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 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:0500059HP:0500059Retinopathy of prematurity zone I0 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.