Global Variome shared LOVD

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Phenotype #0000084268 Individual ID 00106464 Associated disease CMYO4A;CFTD Phenotype details EM: CFTD with possible minicores, decreased fetal movements, hypotonia, joint laxity, ambulant and able to climb stairs; CPK: 53 Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Thomas Cullup Database submission license No license selected Created by Thomas Cullup Date created 2012-09-18 11:57:27 +02:00 (CEST) Date last edited N/A

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