Phenotype #0000350872

Individual ID 00465320
Associated disease USH1F
Phenotype details congenital bilateral hearing loss and first began to experience night blindness when the proband was about 10 years old
Diagnosis/Initial USH
Inheritance Familial, autosomal recessive
Diagnosis/Definite USH1F
Age/Examination 26y (26 years)
Age/Diagnosis 26y
Age/Onset congenital
Phenotype/Onset congenital
Protein We
Owner name Yanbao Xiang
Database submission license No license selected
Created by Yanbao Xiang
Date created 2025-05-13 10:12:45 +02:00 (CEST)
Date last edited 2025-05-14 09:27:40 +02:00 (CEST)

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