Global Variome shared LOVD

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Phenotype #0000301936 Individual ID 00409821 Associated disease WHSUS;MRD37 Phenotype details Delayed speech and language development, Cryptorchidism, Mild microcephaly, Brachycephaly, Gait disturbance Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 04y (4 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2022-05-11 12:12:34 +02:00 (CEST) Date last edited 2022-05-16 10:23:36 +02:00 (CEST)

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