Global Variome shared LOVD

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

Phenotype #0000187414 Individual ID 00248423 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details HP:0012759 (Neurodevelopmental abnormality); HP:0011458 (Abdominal symptom); HP:0002013 (Vomiting); HP:0002066 (Gait ataxia); HP:0100022 (Abnormality of movement); HP:0001627 (Abnormality of cardiac morphology); HP:0001637 (Abnormality of the myocardium); HP:0012547 (Abnormal involuntary eye movements); HP:0001263 (Global developmental delay); HP:0000666 (Horizontal nystagmus) Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2019-07-23 18:22:51 +02:00 (CEST) Date last edited 2019-09-30 12:26:24 +02:00 (CEST)

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