Phenotype #0000326642

Individual ID 00436465
Associated disease STGD4
Phenotype details Photophobia HP:0000613, Reduced visual acuity HP:0007663, Large central visual field defect HP:0001129, Color vision defect HP: 0000551, Central scotoma HP: 0000603, Abnormality of macular pigmentation HP: 0008002
Diagnosis/Initial Stargardt
Inheritance Familial, autosomal recessive
Diagnosis/Definite STGD4
Age/Examination 10y (10 years)
Age/Diagnosis 22y
Age/Onset 05y
Phenotype/Onset -
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 2023-09-17 05:07:47 +02:00 (CEST)
Date last edited 2023-09-18 16:35:17 +02:00 (CEST)

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