Global Variome shared LOVD

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

Phenotype #0000053375 Individual ID 00073639 Associated disease MYOP Phenotype details muscular hypotrophy and hypotonia, psychomotor delay, ID, congenital cataract,lactic acidosis, mitochondrial disorders Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Sophie Nambot Database submission license No license selected Created by Sophie Nambot Date created 2016-06-13 11:32:56 +02:00 (CEST) Date last edited 2016-06-17 11:37:23 +02:00 (CEST)

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