Human Phenotype Ontology 
Grandparent Node:
expandRetinopathy (HP:0000488)help
Parent Node:
expandRetinopathy of prematurity (HP:0500049)help
..Starting node
..expandRetinopathy of prematurity prethreshold (HP:0500065)help
Term ID: 500065
Name: Retinopathy of prematurity prethreshold
Synonym: ROP prethreshold
Definition: High risk patients who were in Zone 1 (no Plus or stage 3) or Zone 2 with Plus or stage 3 but not both.
Comments:
Reference: HP:0500065
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 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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500065HP:0500065Retinopathy of prematurity prethreshold0 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.