Phenotype #0000230590

Individual ID 00303513
Associated disease DFNB9;AUNB1
Phenotype details HP:0008527 Congenital sensorineural hearing impairment
Profound deafness auditory neuropathy
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Sophie Achard
Database submission license No license selected
Created by Sophie Achard
Date created 2020-06-15 15:46:03 +02:00 (CEST)
Date last edited 2020-06-15 17:07:42 +02:00 (CEST)

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