Global Variome shared LOVD

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

Phenotype #0000161988 Individual ID 00213534 Associated disease MYOP Diagnosis/Initial congenital myopathy Diagnosis/Definite - Phenotype details mild proximal weakness, difuse hypotonia, abnormal gait Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Tom Winder Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2013-01-15 21:19:12 +01:00 (CET) Date last edited 2013-01-17 21:10:36 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.