Global Variome shared LOVD

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Phenotype #0000180222 Individual ID 00240057 Associated disease WMS3 Phenotype details Ectopia Lentis, microspherophakia, shallow anterior chamber-severe myopia, short stature, brachydactyly, joint stiffness, pulmonary stenosis, aortic stenosis Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 00d Phenotype/Onset - Protein - Owner name Ramona Haji-Seyed-Javadi Database submission license No license selected Created by Ramona Haji-Seyed-Javadi Date created 2012-02-21 21:30:25 +01:00 (CET) Date last edited 2012-02-22 09:51:33 +01:00 (CET)

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