Human Phenotype Ontology 
Grandparent Node:
expandCochlear malformation (HP:0008554)help
Parent Node:
expandIncomplete partition of the cochlea (HP:0011373)help
..Starting node
..expandIncomplete partition of the cochlea type I (HP:0011374)help
Term ID: 11374
Name: Incomplete partition of the cochlea type I
Synonym:
Definition: Incomplete partition I is also known as cystic cochleovestibular malformation, where the cochlea has no bony modiolus, resulting in an empty cystic cochlea. This is accompanied by a dilated cystic vestibule with developmental arrest at the fifth week of gestation.
Comments:
Reference: HP:0011374
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandIncomplete partition of the cochlea type II (HP:0000376) 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:0011374HP:0011374Incomplete partition of the cochlea type I0 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.