Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the outer ear (HP:0000356)help
Parent Node:
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Abnormal location of ears (HP:0000357)help
Parent Node:
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Abnormal pinna morphology (HP:0000377)help
..Starting node
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Asymmetry of the ears (HP:0010722)help
Term ID: 10722
Name: Asymmetry of the ears
Synonym: Asymmetric ears
Definition: An asymmetriy, i.e., difference in size, shape or position between the left and right ear.
Comments:
Reference: HP:0010722
Genes and Diseases:
 
       Child Nodes:
........expandAsymmetry of the size of ears (HP:0040091) help
........expandAsymmetry of the shape of the ears (HP:0040092) help
........expandAsymmetry of the position of the ears (HP:0040093) help

 Sister Nodes: 
..expandAbnormal antihelix morphology (HP:0009738) help
..expandAbnormal antitragus morphology (HP:0009896) help
..expandAbnormal earlobe morphology (HP:0000363) help
..expandAbnormal helix morphology (HP:0011039) help
..expandAbnormal number of tubercles (HP:0040112) help
..expandAbnormal tragus morphology (HP:0009912) help
..expandAuricular pit (HP:0030025) help
..expandAuricular tag (HP:0030021) help
..expandCalcification of the auricular cartilage (HP:0005103) help
..expandChondritis of pinna (HP:0200047) help
..expandCrumpled ear (HP:0009901) help
..expandCryptotia (HP:0011252) help
..expandCupped ear (HP:0000378) help
..expandCystic lesions of the pinnae (HP:0010723) help
..expandHypoplasia of the ear cartilage (HP:0100720) help
..expandLong ear (HP:0400004) help
..expandLop ear (HP:0000394) help
..expandMacrotia (HP:0000400) help
..expandMicrotia (HP:0008551) help
..expandMozart ear (HP:0030677) help
..expandProtruding ear (HP:0000411) help
..expandQuelprud nodule (HP:0030023) help
..expandQuestion mark ear (HP:0030022) help
..expandRound ear (HP:0100830) help
..expandSatyr ear (HP:0030676) help
..expandShort ear (HP:0400005) help
..expandThickened ears (HP:0009894) 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:0010722HP:0010722Asymmetry of the ears0ASH1L CL E G H5587019088OMIM:617796Mental retardation, autosomal dominant 521
HP:0010722HP:0010722Asymmetry of the ears0BCOR CL E G H5488020893OMIM:300166Microphthalmia, syndromic 2.101
HP:0010722HP:0010722Asymmetry of the ears0GAD1 CL E G H25714092OMIM:619124DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 89; DEE8944
HP:0010722HP:0010722Asymmetry of the ears0PUF60 CL E G H2282717042ORPHA:5084888q24.3 microdeletion syndromeHP:0040282 - Frequent19
HP:0010722HP:0010722Asymmetry of the ears0RAB3GAP2 CL E G H2578217168OMIM:614225Warburg micro syndrome 2.135
HP:0010722HP:0010722Asymmetry of the ears0SMS CL E G H661111123ORPHA:3063X-linked intellectual disability, Snyder typeHP:0040283 - Occasional19
HP:0010722HP:0040093Asymmetry of the position of the ears1 CL E G H
HP:0010722HP:0040092Asymmetry of the shape of the ears1 CL E G H
HP:0010722HP:0040091Asymmetry of the size of ears1 CL E G H


Genes (6) :ASH1L BCOR GAD1 PUF60 RAB3GAP2 SMS

Diseases (6) :OMIM:617796 OMIM:300166 OMIM:619124 ORPHA:508488 OMIM:614225 ORPHA:3063
 

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