Global Variome shared LOVD

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Phenotype #0000172886 Individual ID 00229664 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Developmental delay (HP:0001263), Intellectual disability (HP:0001249), Muscular hypotonia (HP:0001252), Seizures (HP:0001250) Inheritance Isolated (sporadic) Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Pauline E Schneeberger Database submission license No license selected Created by Pauline E Schneeberger Date created 2019-04-08 14:55:36 +02:00 (CEST) Date last edited 2019-04-09 07:34:08 +02:00 (CEST)

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