Global Variome shared LOVD

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

Phenotype #0000188503 Individual ID 00249627 Associated disease FHBL1 Phenotype details Also has spastic paraplegia (SPG11) Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis 30y Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license No license selected Created by Amanda Hooper Date created 2015-06-16 03:46:06 +02:00 (CEST) Date last edited N/A

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