Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormality of the outer ear (HP:0000356)

Parent Node:
Abnormality of the auditory canal (HP:0000372)

..Starting node
..Cerumen abnormality (HP:0030787)

Term ID:

30787

Name:

Cerumen abnormality

Synonym:

Definition:

Any anomaly of the cerumen (ear wax), the yellowish waxy substance secreted in the ear canal.

Comments:

Reference:

HP:0030787

Genes and Diseases:

Child Nodes:

........

Impacted cerumen (HP:0030788)

........

Excessive cerumen (HP:0030789)

........

Abnormal cerumen color (HP:0030790)

Sister Nodes:

Atresia of the external auditory canal (HP:0000413)

Exostosis of the external auditory canal (HP:0004459)

Otitis externa (HP:0410017)

Stenosis of the external auditory canal (HP:0000402)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030787	HP:0030787	Cerumen abnormality	0	CL E G H
HP:0030787	HP:0030788	Impacted cerumen	1	CL E G H
HP:0030787	HP:0030790	Abnormal cerumen color	1	CL E G H
HP:0030787	HP:0030789	Excessive cerumen	1	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.