Human Phenotype Ontology 
Grandparent Node:
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Abnormality of male external genitalia (HP:0000032)help
Parent Node:
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Abnormal testis morphology (HP:0000035)help
..Starting node
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Orchitis (HP:0100796)help
Term ID: 100796
Name: Orchitis
Synonym: Inflammation of testicles
Definition: Testicular inflammation.
Comments:
Reference: HP:0100796
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of the Leydig cells (HP:0010789) help
..expandAbnormality of the testis size (HP:0045058) help
..expandAnorchism (HP:0030869) help
..expandCryptorchidism (HP:0000028) help
..expandDysplastic testes (HP:0008733) help
..expandHydrocele testis (HP:0000034) help
..expandIntratesticular abscess (HP:0025038) help
..expandMonorchism (HP:0030868) help
..expandPrimary testicular failure (HP:0008720) help
..expandRetractile testis (HP:0012646) help
..expandSupernumerary testes (HP:0010470) help
..expandTesticular atrophy (HP:0000029) help
..expandTesticular dysgenesis (HP:0008715) help
..expandTesticular fibrosis (HP:0012860) help
..expandTesticular lipomatosis (HP:0025476) help
..expandTesticular microlithiasis (HP:0012215) help
..expandTesticular neoplasm (HP:0010788) help
..expandTesticular torsion (HP:0100813) help
..expandVanishing testis (HP:0012870) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100796HP:0100796Orchitis0C4A CL E G H7201323ORPHA:117Behçet diseaseHP:0040281 - Very frequent1
HP:0100796HP:0100796Orchitis0CCR1 CL E G H12301602ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0100796HP:0100796Orchitis0ERAP1 CL E G H5175218173ORPHA:117Behçet diseaseHP:0040281 - Very frequent1
HP:0100796HP:0100796Orchitis0FAS CL E G H35511920ORPHA:117Behçet diseaseHP:0040281 - Very frequent59
HP:0100796HP:0100796Orchitis0HLA-B CL E G H31064932ORPHA:117Behçet diseaseHP:0040281 - Very frequent4
HP:0100796HP:0100796Orchitis0IFNGR1 CL E G H34595439ORPHA:117Behçet diseaseHP:0040281 - Very frequent60
HP:0100796HP:0100796Orchitis0IL10 CL E G H35865962ORPHA:117Behçet diseaseHP:0040281 - Very frequent2
HP:0100796HP:0100796Orchitis0IL12A CL E G H35925969ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0100796HP:0100796Orchitis0IL12A-AS1 CL E G H10192837649094ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0100796HP:0100796Orchitis0IL23R CL E G H14923319100ORPHA:117Behçet diseaseHP:0040281 - Very frequent1
HP:0100796HP:0100796Orchitis0KLRC4 CL E G H83026377ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0100796HP:0100796Orchitis0MEFV CL E G H42106998ORPHA:117Behçet diseaseHP:0040281 - Very frequent281
HP:0100796HP:0100796Orchitis0MEFV CL E G H42106998ORPHA:342Familial Mediterranean feverHP:0040283 - Occasional281
HP:0100796HP:0100796Orchitis0MEFV CL E G H42106998OMIM:249100Familial Mediterranean fever, AR281
HP:0100796HP:0100796Orchitis0STAT4 CL E G H677511365ORPHA:117Behçet diseaseHP:0040281 - Very frequent2
HP:0100796HP:0100796Orchitis0TLR4 CL E G H709911850ORPHA:117Behçet diseaseHP:0040281 - Very frequent3
HP:0100796HP:0100796Orchitis0TNFRSF1A CL E G H713211916ORPHA:32960Tumor necrosis factor receptor 1 associated periodic syndromeHP:0040282 - Frequent131
HP:0100796HP:0100796Orchitis0UBAC2 CL E G H33786720486ORPHA:117Behçet diseaseHP:0040281 - Very frequent


Genes (16) :C4A CCR1 ERAP1 FAS HLA-B IFNGR1 IL10 IL12A IL12A-AS1 IL23R KLRC4 MEFV STAT4 TLR4 TNFRSF1A UBAC2

Diseases (4) :ORPHA:117 ORPHA:342 OMIM:249100 ORPHA:32960
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.