Global Variome shared LOVD

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Phenotype #0000010356 Individual ID 00011663 Associated disease SPG Phenotype details hereditary spastic paraplegia, type 47 (SPG-47); see article Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2014-02-16 11:18:19 +01:00 (CET) Date last edited 2014-02-16 11:25:53 +01:00 (CET)

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