Global Variome shared LOVD

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Phenotype #0000125198 Individual ID 00102397 Associated disease MDC Phenotype details Muscular hypotonia (HP:0001252), Abnormality of the cerebral white matter (HP:0002500) Diagnosis/Initial dystrophy, muscular, congenital Diagnosis/Definite MDC-1A Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Tom Winder Database submission license No license selected Created by Tom Winder Date created 2010-03-04 16:44:42 +01:00 (CET) Date last edited 2017-10-08 00:02:26 +02:00 (CEST)

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