Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal uvea morphology (HP:0000553)help
Grandparent Node:
expand
Inflammatory abnormality of the eye (HP:0100533)help
Parent Node:
expand
Uveitis (HP:0000554)help
..Starting node
..expand
Anterior uveitis (HP:0012122)help
Term ID: 12122
Name: Anterior uveitis
Synonym:
Definition: Inflammation of the uveal tract in which the primary site of inflammation is the anterior chamber.
Comments:
Reference: HP:0012122
Genes and Diseases:
 
       Child Nodes:
........expandIridocyclitis (HP:0001094) help

 Sister Nodes: 
..expandIntermediate uveitis (HP:0012124) help
..expandNongranulomatous uveitis (HP:0007813) 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:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012122HP:0012122Anterior uveitis0HLA-DRB1 CL E G H312385414ORPHA026194948142857
HP:0012122HP:0012122Anterior uveitis0IL6 CL E G H356985414ORPHA09386018147620
HP:0012122HP:0012122Anterior uveitis0LACC1 CL E G H14481185414ORPHA034926789613409
HP:0012122HP:0012122Anterior uveitis0MIF CL E G H428285414ORPHA041147097153620
HP:0012122HP:0012122Anterior uveitis0TNFAIP3 CL E G H7128616744Autoinflammatory syndrome, familial, Behcet-like616744C4225218OMIM0315511896191163
HP:0012122HP:0012122Anterior uveitis1HLA-DRB1 CL E G H312385414ORPHA026194948142857
HP:0012122HP:0012122Anterior uveitis1IL6 CL E G H356985414ORPHA09386018147620
HP:0012122HP:0012122Anterior uveitis1LACC1 CL E G H14481185414ORPHA034926789613409
HP:0012122HP:0012122Anterior uveitis1MIF CL E G H428285414ORPHA041147097153620
HP:0012122HP:0012122Anterior uveitis1TNFAIP3 CL E G H7128616744Autoinflammatory syndrome, familial, Behcet-like616744C4225218OMIM0315511896191163


Genes (14) :ANKRD55 CD247 HLA-DRB1 IL2RA IL2RB IL6 LACC1 MIF NOD2 PTPN2 PTPN22 STAT4 STUB1 TNFAIP3

Diseases (5) :85414 616744 85410 90340 412057
 

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