Global Variome shared LOVD

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Phenotype #0000306884 Individual ID 00415083 Associated disease WHS Phenotype details Global developmental delay, Axial hypotonia, Failure to thrive, Microcephaly, Short stature, Retrognathia, Omphalocele, Elevated circulating creatine kinase concentration, Epicanthus Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - 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 2022-08-08 07:29:43 +02:00 (CEST) Date last edited 2022-08-13 17:18:58 +02:00 (CEST)

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