Phenotype #0000230457

Individual ID 00303381
Associated disease HL
Phenotype details see paper; ..., unilateral cochlear nerve aplasia
Diagnosis/Initial hearing loss
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-06-11 13:51:54 +02:00 (CEST)
Date last edited 2020-06-11 13:54:28 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.