Global Variome shared LOVD

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Phenotype #0000308486 Individual ID 00416975 Associated disease ROP Phenotype details no hearing impairment Diagnosis/Initial - Inheritance Familial, X-linked Diagnosis/Definite retinopathy of prematurity Age/Examination - Age/Onset 5m Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-09-12 11:14:36 +02:00 (CEST) Date last edited N/A

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