Global Variome shared LOVD

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

Phenotype #0000093276 Individual ID 00117895 Associated disease AOA3 Phenotype details truncal ataxia with impaired ocular movement, elevated alpha-fetoprotein levels Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 14y Phenotype/Onset - Protein - Owner name Nada Al Tassan Database submission license No license selected Created by Nada Al Tassan Date created 2011-10-18 13:53:58 +02:00 (CEST) Date last edited 2019-12-20 08:49:52 +01:00 (CET)

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