Global Variome shared LOVD

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

Phenotype #0000161996 Individual ID 00213542 Associated disease NEM Phenotype details distal weakness lowerlimbs; wheelchair bound >40y Diagnosis/Initial nemaline myopathy Inheritance Familial, autosomal dominant Diagnosis/Definite NEM-4 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - 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 12:28:19 +02:00 (CEST) Date last edited 2013-08-31 16:36:37 +02:00 (CEST)

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