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