Human Phenotype Ontology 
Grandparent Node:
expandAbnormal vascular morphology (HP:0025015)help
Parent Node:
expandAbnormal systemic arterial morphology (HP:0011004)help
..Starting node
..expandArteritis (HP:0012089)help
Term ID: 12089
Name: Arteritis
Synonym: Inflammation of artery
Definition: Arterial inflammation.
Comments:
Reference: HP:0012089
Genes and Diseases:
 
       Child Nodes:
........expandGranulomatous coronary arteritis (HP:0006679) help
........expandRetinal arteritis (HP:0008030) help

 Sister Nodes: 
..expandAbnormal aortic morphology (HP:0001679) help
..expandAbnormal carotid artery morphology (HP:0005344) help
..expandAbnormal celiac artery morphology (HP:0012326) help
..expandAbnormal cerebral artery morphology (HP:0009145) help
..expandAbnormal coronary artery morphology (HP:0006704) help
..expandAbnormal facial artery morphology (HP:3000024) help
..expandAbnormal greater palatine artery morphology (HP:3000049) help
..expandAbnormal lacrimal artery morphology (HP:3000065) help
..expandAbnormal lingual artery morphology (HP:3000074) help
..expandAbnormal radial artery morphology (HP:0031640) help
..expandAbnormal renal artery morphology (HP:0008776) help
..expandAbnormal retinal artery morphology (HP:0000630) help
..expandAbnormal subclavian artery morphology (HP:0031251) help
..expandAbnormal vertebral artery morphology (HP:0030321) help
..expandArterial calcification (HP:0003207) help
..expandArterial dissection (HP:0005294) help
..expandArterial fibromuscular dysplasia (HP:0005313) help
..expandArterial intimal fibrosis (HP:0011353) help
..expandArterial stenosis (HP:0100545) help
..expandArterial tortuosity (HP:0005116) help
..expandArteriosclerosis (HP:0002634) help
..expandCystic medial necrosis (HP:0012180) help
..expandDilatation of an abdominal artery (HP:0002636) 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:0012089HP:0012089Arteritis0HYOU1 CL E G H1052516931OMIM:233600Immunodeficiency 59 and hypoglycemia.
HP:0012089HP:0012089Arteritis0UBA1 CL E G H731712469OMIM:301054VEXAS SYNDROME; VEXAS35
HP:0012089HP:0008030Retinal arteritis1 CL E G H
HP:0012089HP:0006679Granulomatous coronary arteritis1 CL E G H


Genes (2) :HYOU1 UBA1

Diseases (2) :OMIM:233600 OMIM:301054
 

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