Global Variome shared LOVD

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Phenotype #0000026563 Individual ID 00033134 Associated disease - Phenotype details retinal degeneration, severe, early onset (EOSRD); Leber congenital amaurosis; mild intellectual disability Diagnosis/Initial retinitis pigmentosa Inheritance Unknown Diagnosis/Definite - Age/Examination 0d Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Kornelia Neveling Database submission license No license selected Created by Kornelia Neveling Date created 2012-02-04 14:52:54 +01:00 (CET) Date last edited 2020-08-25 10:48:31 +02:00 (CEST)

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