Global Variome shared LOVD

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Phenotype #0000203223 Individual ID 00265415 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Global developmental delay (HP:0001263); Hypopigmentation of the skin (HP:0001010); Agenesis of corpus callosum (HP:0001274); Strabismus (HP:0000486); Red hair (HP:0002297); Focal seizures (HP:0007359) 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 2019-09-25 09:36:59 +02:00 (CEST) Date last edited 2019-09-30 12:26:24 +02:00 (CEST)

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