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 InternationalCreative Commons License
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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