Phenotype #0000278802

Individual ID 00385018
Associated disease -
Phenotype details no nyctalopia/photophobia, nystagmus, ERG extinguished, best corrected visual acuity right/left eye: HM/HM
Diagnosis/Initial Leber congenital amaurosis
Inheritance Isolated (sporadic)
Diagnosis/Definite Leber congenital amaurosis
Age/Examination 26y (26 years)
Age/Diagnosis -
Age/Onset 1y
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-10-06 17:52:46 +02:00 (CEST)
Date last edited N/A

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