Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000162051 Individual ID 00213597 Associated disease MYOP Phenotype details axial weakness, neck flexor weakness, mildly rigid spine, lumbar hyperlordosis, mild proximal weakness Diagnosis/Initial cap myopathy Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 3m Phenotype/Onset weakness neck flexor Protein - Owner name Minttu Marttila Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2013-08-28 14:23:47 +02:00 (CEST) Date last edited 2013-08-31 16:53:59 +02:00 (CEST)

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