Phenotype #0000326755

Individual ID 00436608
Associated disease WFSL
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, Optic atrophy HP:0000648
Diagnosis/Initial Usher syndrome
Inheritance Familial, autosomal dominant
Diagnosis/Definite # 614296
Age/Examination 13y (13 years)
Age/Diagnosis 50y
Age/Onset 13y
Phenotype/Onset 13y
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 2023-09-23 06:21:34 +02:00 (CEST)
Date last edited 2023-09-28 19:30:22 +02:00 (CEST)

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