Global Variome shared LOVD

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

Phenotype #0000207793 Individual ID 00271177 Associated disease TAM1 Phenotype details Upper and lower limb muscle weakness, eye movement defects, contractures Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset Childhood Protein - Owner name Johann Böhm Database submission license No license selected Created by Johann Böhm Date created 2019-12-13 16:18:01 +01:00 (CET) Date last edited N/A

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