Phenotype #0000326600

Individual ID 00436419
Associated disease CLN3
Inheritance Familial, autosomal recessive
Diagnosis/Initial 20y
Age/Examination 20y, 70y
Diagnosis/Definite -
Age/Diagnosis 70y
Age/Onset 20y
Phenotype/Onset 20y
Phenotype details Reduced visual acuity HP:0007663, Nyctalopia HP:0000662, Peripheral visual field loss HP:0007994, Retinitis pigmentosa HP:0000510
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 2023-09-14 17:43:25 +02:00 (CEST)
Date last edited 2023-09-18 16:35:17 +02:00 (CEST)

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