Human Phenotype Ontology 
Grandparent Node:
expandAbnormal morphology of the great vessels (HP:0030962)help
Grandparent Node:
expandAbnormal systemic arterial morphology (HP:0011004)help
Parent Node:
expandAbnormal aortic morphology (HP:0001679)help
..Starting node
..expandDescending aorta hypoplasia (HP:0025495)help
Term ID: 25495
Name: Descending aorta hypoplasia
Synonym:
Definition: Significant luminal narrowing of a long segment of the descending aorta.
Comments:
Reference: HP:0025495
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal aortic arch morphology (HP:0012303) help
..expandAbnormal ascending aorta morphology (HP:0031784) help
..expandAortic aneurysm (HP:0004942) help
..expandAortic atherosclerotic lesion (HP:0012397) help
..expandAortic dissection (HP:0002647) help
..expandAortic rupture (HP:0031649) help
..expandAortic tortuosity (HP:0006687) help
..expandAorto-ventricular tunnel (HP:0011627) help
..expandAortopulmonary collateral arteries (HP:0031834) help
..expandCalcification of the aorta (HP:0004963) help
..expandCoarctation of aorta (HP:0001680) help
..expandCoated aorta (HP:0025494) help
..expandMucoid extracellular matrix accumulation (HP:0200146) help
..expandOverriding aorta (HP:0002623) help
..expandPenetrating aortic ulcer (HP:0031648) 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:0025495HP:0025495Descending aorta hypoplasia0 CL E G H


Genes (0) :

Diseases (0) :
 

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