Global Variome shared LOVD

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Phenotype #0000001869 Individual ID 00003018 Associated disease IBMPFD1 Phenotype details hereditary spastic paraplegia Diagnosis/Initial hereditary spastic paraplegia Inheritance Isolated (sporadic) Diagnosis/Definite IBMPFD Age/Examination - Age/Diagnosis - Age/Onset 06y Phenotype/Onset - Protein - Owner name Marcel Nelen Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2013-10-02 11:35:03 +02:00 (CEST) Date last edited 2022-11-17 09:49:29 +01:00 (CET)

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