Human Phenotype Ontology 
Grandparent Node:
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Abnormal uvea morphology (HP:0000553)help
Grandparent Node:
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Inflammatory abnormality of the eye (HP:0100533)help
Parent Node:
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Uveitis (HP:0000554)help
..Starting node
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Nongranulomatous uveitis (HP:0007813)help
Term ID: 7813
Name: Nongranulomatous uveitis
Synonym:
Definition: A form of uveitis that is not associated with the formation of granulomas.
Comments:
Reference: HP:0007813
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAnterior uveitis (HP:0012122) help
..expandIntermediate uveitis (HP:0012124) help
..expandPanuveitis (HP:0012121) help
..expandPosterior uveitis (HP:0012123) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007813HP:0007813Nongranulomatous uveitis0NOD2 CL E G H64127186580Blau syndrome186580C1861303OMIM11214425331605956
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :NOD2

Diseases (1) :186580
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.