Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000087312 Individual ID 00111199 Associated disease SPG Phenotype details motor neuropathy, ID, mild ataxia Diagnosis/Initial hereditary spastic paraplegia Inheritance Familial, autosomal recessive Diagnosis/Definite SPAX5 Age/Examination 05y (5 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Erik-Jan Kamsteeg Database submission license No license selected Created by Erik-Jan Kamsteeg Date created 2015-11-24 13:58:38 +01:00 (CET) Date last edited 2022-11-17 16:03:33 +01:00 (CET)

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