Global Variome shared LOVD

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Phenotype #0000001759 Individual ID 00002845 Associated disease SPG17 Phenotype details spastic paraplegia (SP); Silver Syndrome (SS); CMT2; variability among patients, all spectrum of phenotype: pure SP, SS, CMT2 Diagnosis/Initial - Inheritance Familial Diagnosis/Definite - Age/Onset - Phenotype/Onset - Age/Diagnosis - Age/Examination - Protein - Owner name María-Jesús Sobrido Database submission license No license selected Created by María-Jesús Sobrido Date created 2012-03-24 15:06:53 +01:00 (CET) Date last edited N/A

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