Global Variome shared LOVD

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Phenotype #0000106258 Individual ID 00133511 Associated disease LGMDR5;LGMD2C Phenotype details - Diagnosis/Initial severe autosomal recessive muscular dystrophy, North African type (SCARMD) Inheritance Familial Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Marina Fanin Database submission license No license selected Created by Marina Fanin Date created 2014-12-11 11:04:32 +01:00 (CET) Date last edited 2014-12-12 10:54:32 +01:00 (CET)

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