Human Phenotype Ontology 
Grandparent Node:
Abnormal choroid morphology (HP:0000610)help
Grandparent Node:
Abnormal retinal morphology (HP:0000479)help
Parent Node:
Abnormal chorioretinal morphology (HP:0000532)help
..Starting node
Chorioretinitis (HP:0012424)help
Term ID: 12424
Name: Chorioretinitis
Definition: An inflammation of the choroid and retina.
Reference: HP:0012424
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of chorioretinal pigmentation (HP:0007661) help
..expandCentral serous chorioretinopathy (HP:0025567) help
..expandChorioretinal coloboma (HP:0000567) help
..expandChorioretinal degeneration (HP:0200065) help
..expandChorioretinal dysplasia (HP:0007731) help
..expandChorioretinal dystrophy (HP:0001135) help
..expandChorioretinal lacunae (HP:0007858) 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:0012424HP:0012424Chorioretinitis0 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 June 2019 release.