Global Variome shared LOVD

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

Phenotype #0000204089 Individual ID 00266312 Associated disease CMS Phenotype details HP:0003198 (Myopathy), HP:0001319 (Neonatal hypotonia) Diagnosis/Initial 0y Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2019-10-22 14:21:40 +02:00 (CEST) Date last edited 2019-10-22 19:42:28 +02:00 (CEST)

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