Human Phenotype Ontology 
Grandparent Node:
expandAbnormal vascular morphology (HP:0025015)help
Parent Node:
expandAbnormal systemic arterial morphology (HP:0011004)help
..Starting node
..expandArterial intimal fibrosis (HP:0011353)help
Term ID: 11353
Name: Arterial intimal fibrosis
Synonym: Intimal fibrosis
Definition: Formation of excess fibrous connective tissue in the tunica intima (innermost layer) of arteries.
Comments:
Reference: HP:0011353
Genes and Diseases:
 
       Child Nodes:

 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 stenosis (HP:0100545) help
..expandArterial tortuosity (HP:0005116) help
..expandArteriosclerosis (HP:0002634) help
..expandArteritis (HP:0012089) 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:0011353HP:0011353Arterial intimal fibrosis0BMPR2 CL E G H6591078OMIM:178600Pulmonary hypertension, primary, 1.525


Genes (1) :BMPR2

Diseases (1) :OMIM:178600
 

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