Global Variome shared LOVD

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Phenotype #0000093282 Individual ID 00117901 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Diffuse cerebral hypomyelination with cerebellar atrophy, hypoplasia of corpus callosum; HCAHC Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Gerard C.P. Schaafsma Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2011-12-01 15:36:32 +01:00 (CET) Date last edited N/A

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