Human Phenotype Ontology 
Grandparent Node:
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Abnormal respiratory system physiology (HP:0002795)help
Parent Node:
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Abnormal pattern of respiration (HP:0002793)help
..Starting node
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Hypopnea (HP:0040213)help
Term ID: 40213
Name: Hypopnea
Synonym: Shallow breathing
Definition: Hypopnea is referring to breathing that is abnormally shallow.
Comments:
Reference: HP:0040213
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandApnea (HP:0002104) help
..expandCheyne-Stokes respiration (HP:0012196) help
..expandHyperventilation (HP:0002883) help
..expandHypoventilation (HP:0002791) help
..expandIrregular respiration (HP:0012195) help
..expandNight gasping (HP:0031503) help
..expandParadoxical respiration (HP:0030207) help
..expandTachypnea (HP:0002789) 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:0040213HP:0040213Hypopnea0HTRA2 CL E G H2742914348OMIM:6172483-methylglutaconic aciduria, type VIII39
HP:0040213HP:0040213Hypopnea0MYO1H CL E G H28344613879OMIM:619482CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 2, AND AUTONOMIC DYSFUNCTION; CCHS2
HP:0040213HP:0040213Hypopnea0TMEM218 CL E G H21985427344OMIM:619562JOUBERT SYNDROME 39; JBTS39


Genes (3) :HTRA2 MYO1H TMEM218

Diseases (3) :OMIM:617248 OMIM:619482 OMIM:619562
 

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