Human Phenotype Ontology 
Grandparent Node:
Abnormal uvea morphology (HP:0000553)help
Grandparent Node:
Inflammatory abnormality of the eye (HP:0100533)help
Parent Node:
Uveitis (HP:0000554)help
..Starting node
Nongranulomatous uveitis (HP:0007813)help
Term ID: 7813
Name: Nongranulomatous uveitis
Definition: A form of uveitis that is not associated with the formation of granulomas.
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 syndrome186580C1861303OMIM15615331605956
HP:0007813HP:0007813Nongranulomatous uveitis0NOD2 CL E G H64127186580Blau syndrome186580C1861303OMIM16535331605956
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 August 2021 release.