Phenotype #0000326729

Individual ID 00436578
Associated disease USH2A
Phenotype details Reduced visual acuity HP:0007663, Nyctalopia HP:0000662, Peripheral visual field loss HP:0007994, Retinitis pigmentosa HP:0000510, Moderate sensorineural hearing impairment HP:0008504
Diagnosis/Initial Usher syndrome
Inheritance Familial, autosomal recessive
Diagnosis/Definite # 276901
Age/Examination 15y (15 years)
Age/Diagnosis 55y
Age/Onset 15y
Phenotype/Onset 15y
Protein -
Owner name Rocio Villafuerte-de la Cruz
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Rocio Villafuerte-de la Cruz
Date created 2023-09-21 21:14:31 +02:00 (CEST)
Date last edited 2023-09-22 14:36:43 +02:00 (CEST)

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