Human Phenotype Ontology 
Grandparent Node:
Behavioral abnormality (HP:0000708)help
Parent Node:
Abnormal respiratory system physiology (HP:0002795)help
Parent Node:
Sleep disturbance (HP:0002360)help
..Starting node
Snoring (HP:0025267)help
Term ID: 25267
Name: Snoring
Synonym: Snore; Snores; Snoring symptoms
Definition: Deep, noisy breathing during sleep accompanied by hoarse or harsh sounds caused by the vibration of respiratory structures (especially the soft palate) resulting in sound due to obstructed air movement during breathing while sleeping.
Reference: HP:0025267
Genes and Diseases:
       Child Nodes:
........expandLoud snoring (HP:0025372) help

 Sister Nodes: 
..expandAbnormal rapid eye movement sleep (HP:0002494) help
..expandBruxism (HP:0003763) help
..expandExcessive daytime somnolence (HP:0001262) help
..expandHypersomnia (HP:0100786) help
..expandInsomnia (HP:0100785) help
..expandNarcolepsy (HP:0030050) help
..expandobsolete Excessive daytime sleepiness (HP:0002189) help
..expandParasomnia (HP:0025234) help
..expandRestless legs (HP:0012452) help
..expandSleep apnea (HP:0010535) help
..expandSleep paralysis (HP:0025233) help
..expandSleep-wake cycle disturbance (HP:0006979) 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:0025267HP:0025267Snoring0AHDC1 CL E G H2724525230ORPHA:412069AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndromeHP:0040283 - Occasional36
HP:0025267HP:0025267Snoring0AHDC1 CL E G H2724525230OMIM:615829Xia-Gibbs syndrome.36
HP:0025267HP:0025267Snoring0EDN1 CL E G H19063176ORPHA:137888Auriculocondylar syndromeHP:0040282 - Frequent6
HP:0025267HP:0025267Snoring0GNAI3 CL E G H27734387ORPHA:137888Auriculocondylar syndromeHP:0040282 - Frequent2
HP:0025267HP:0025267Snoring0GNAI3 CL E G H27734387OMIM:602483Auriculocondylar syndrome 1.2
HP:0025267HP:0025267Snoring0GPR101 CL E G H8355014963OMIM:300942Chromosome Xq26.3 duplication syndrome.5
HP:0025267HP:0025267Snoring0GUSB CL E G H29904696OMIM:253220Mucopolysaccharidosis, type VII54
HP:0025267HP:0025267Snoring0HEPHL1 CL E G H34120830477OMIM:261990PILI TORTI AND DEVELOPMENTAL DELAY
HP:0025267HP:0025267Snoring0PLCB4 CL E G H53329059ORPHA:137888Auriculocondylar syndromeHP:0040282 - Frequent82
HP:0025267HP:0025267Snoring0PLCB4 CL E G H53329059OMIM:614669Auriculocondylar syndrome 2.82
HP:0025267HP:0025372Loud snoring1GUSB CL E G H29904696OMIM:253220Mucopolysaccharidosis, type VII54


Diseases (8) :ORPHA:412069 OMIM:615829 ORPHA:137888 OMIM:602483 OMIM:300942 OMIM:253220 OMIM:261990 OMIM:614669

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