Log In|Sign Up
ENNon-Syndromic Genetic Deafness
Alias:
Nonsyndromic Genetic Hearing Loss
Non-Syndromic Genetic Hearing Loss
Isolated Genetic Hearing Loss
Isolated Genetic Deafness
Favorite
Non-Syndromic Genetic Deafness, also known as nonsyndromic genetic hearing loss, is related to deafness, autosomal recessive 1a and sensorineural hearing loss. An important gene associated with Non-Syndromic Genetic Deafness is CDH23 (Cadherin Related 23), and among its related pathways/superpathways are Olfactory Signaling Pathway and RhoGDI Pathway. Affiliated tissues include monocytes and bone, and related phenotypes are delayed speech and language development and progressive sensorineural hearing impairment
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
