Global Variome shared LOVD

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Phenotype #0000051149 Individual ID 00064992 Associated disease ASGD2 Phenotype details congenital primary aphasia as primary phenotype, aplasia of the anterior segment of the eye, iris absent, microphthalmia, retinal dysplasia Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Deepti Anand Database submission license No license selected Created by Johan den Dunnen Date created 2016-05-15 14:36:57 +02:00 (CEST) Date last edited N/A

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