Phenotype #0000293099

Individual ID 00400058
Associated disease USH
Diagnosis/Initial Usher syndrome type 2
Diagnosis/Definite Usher syndrome type 2
Phenotype details Moderate sloping sensorineural hearing loss and retinitis pigmentosa
Inheritance Familial, autosomal recessive
Age/Examination 19y (19 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-01-24 12:26:06 +01:00 (CET)
Date last edited N/A

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