Global Variome shared LOVD

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

Phenotype #0000078638 Individual ID 00100436 Associated disease EIEE Phenotype details severe early infantile encephalopathy (global) hyperkinetic stereotypic movements "oculogyric like" eye movements Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 02y (2 years) Age/Diagnosis - Age/Onset 00y02m Phenotype/Onset - Protein - Intellectual_dis profound Owner name Ronen Spiegel Database submission license No license selected Created by Ronen Spiegel Date created 2017-02-23 22:46:32 +01:00 (CET) Date last edited 2017-03-05 16:23:41 +01:00 (CET)

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