Human Phenotype Ontology 
Grandparent Node:
expandRetinopathy (HP:0000488)help
Parent Node:
expandRetinopathy of prematurity (HP:0500049)help
..Starting node
..expandRetinopathy of prematurity pre-plus (HP:0500063)help
Term ID: 500063
Name: Retinopathy of prematurity pre-plus
Synonym: ROP pre-plus
Definition: As vascular abnormalities of the posterior pole that are insufficient for the diagnosis of plus disease but that demonstrate more arterial tortuosity and more venous dilatation than normal.
Comments:
Reference: HP:0500063
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandRetinopathy of prematurity plus (HP:0500062) 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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500063HP:0500063Retinopathy of prematurity pre-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 December 15 2022 release.