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:
Hearing impairment (HP:0000365)

Parent Node:
Conductive hearing impairment (HP:0000405)

Parent Node:
Mild hearing impairment (HP:0012712)

Parent Node:
Moderate hearing impairment (HP:0012713)

..Starting node
..Moderate conductive hearing impairment (HP:0012716)

Term ID:

12716

Name:

Moderate conductive hearing impairment

Synonym:

Conductive hearing loss, moderate

Definition:

The presence of a moderate form of conductive hearing impairment.

Comments:

Reference:

HP:0012716

Genes and Diseases:

Child Nodes:

Sister Nodes:

Moderate sensorineural hearing impairment (HP:0008504)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012716	HP:0012716	Moderate conductive hearing impairment	0	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.