Global Variome shared LOVD

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Phenotype #0000058659 Individual ID 00078903 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details neuropathy, hereditary sensory, with spastic paraplegia; spastic paraplegia, progressive sensory loss, mutilating acropathy involving both upper/lower limbs; MRI severe atrophy spinal cord predominantly posterior tract Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset early infancy Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2012-10-26 11:36:17 +02:00 (CEST) Date last edited 2012-11-03 11:17:50 +01:00 (CET)

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