Global Variome shared LOVD

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

Phenotype #0000105723 Individual ID 00132962 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Global developmental delay (HP:0001263); Seizures (HP:0001250); Abnormality of movement (HP:0100022); Abnormality of the cerebral cortex (HP:0002538); Sleep disturbance (HP:0002360); Restlessness (HP:0000711) Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name IMGAG Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by IMGAG Date created 2017-11-10 16:51:04 +01:00 (CET) Date last edited 2020-04-01 13:57:49 +02:00 (CEST)

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