Phenotype #0000299331

Individual ID 00406881
Associated disease -
Phenotype details eye movement: pendular nystagmus, vitreous: opacity right eye, macula: atrophy and pigment clumps, white dots: equatorial, spiculation: none
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite Leber congenital amaurosi
Age/Examination 25y (25 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-04-05 15:12:11 +02:00 (CEST)
Date last edited N/A

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