Global Variome shared LOVD

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Phenotype #0000043849 Individual ID 00057161 Associated disease HMN2 Phenotype details neuropathy, distal hereditary motor, type II; exclusive lower motor neuron disease without sensory loss, onset age 15–25y, presenting symptoms paresis extensor muscles big toe later extensor muscles feet, disease progresses rapidly, complete paralysis all distal muscles lower extremities within 5y, EMG chronic neurogenic alterations Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2012-11-05 16:17:39 +01:00 (CET) Date last edited 2016-01-12 06:33:25 +01:00 (CET)

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