Global Variome shared LOVD

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

Phenotype #0000338915 Individual ID 00449770 Associated disease ID Diagnosis/Initial neurodevelopmental delay Diagnosis/Definite BRYLIB2 Inheritance Isolated (sporadic) Phenotype details HP:0001511, HP:0002079, HP:0008058, HP:0000260, HP:0011304, HP:0000365, HP:0001508, HP:0000028, HP:0001998 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Marketa Wayhelova Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Marketa Wayhelova Date created 2024-05-15 06:24:01 +02:00 (CEST) Date last edited 2024-08-20 16:08:24 +02:00 (CEST)

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