Log In|Sign Up
ENHypokalemic Tubulopathy and Deafness (HKTD)
Alias:
Hktd
Favorite
Hypokalemic Tubulopathy and Deafness, is also known as hktd. An important gene associated with Hypokalemic Tubulopathy and Deafness is KCNJ16 (Potassium Inwardly Rectifying Channel Subfamily J Member 16). Related phenotypes are sensorineural hearing impairment and increased circulating renin level
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
