Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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:
Morphological abnormality of the inner ear (HP:0011390)

Parent Node:
Morphological abnormality of the nerves of the inner ear (HP:0011391)

..Starting node
..Abnormality of the cochlear nerve (HP:0011396)

Term ID:

11396

Name:

Abnormality of the cochlear nerve

Synonym:

Definition:

Comments:

Reference:

HP:0011396

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormality of the vestibular nerve (HP:0011392)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011396	HP:0011396	Abnormality of the cochlear nerve	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.