Global Variome shared LOVD

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Phenotype #0000002897 Individual ID 00004105 Associated disease SPG3A Phenotype details scoliosis, urinary symptoms, pes cavus, decreased vibration sense, paresthesia, numbness, excessive tingling Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 45y (45 years) Age/Diagnosis - Age/Onset 01y Phenotype/Onset - Protein - Owner name Tahir Khan Database submission license Creative Commons Attribution 4.0 International Created by Johan den Dunnen Date created 2013-12-20 10:22:29 +01:00 (CET) Date last edited 2017-01-03 16:09:18 +01:00 (CET)

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