Phenotypes for disease #05112 (HMN2 (neuropathy, motor, distal, hereditary, type II (HMN-2)))

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000043154 Neuropathy, distal hereditary motor, type II - - Familial, autosomal dominant - - - - - Johan den Dunnen 00056466
0000043155 neuropathy, distal hereditary motor, type II - - Familial, autosomal dominant - - - - - Johan den Dunnen 00056467
0000043848 Neuropathy, distal hereditary motor, type II - - Familial, autosomal dominant - - - - - Johan den Dunnen 00057160
0000043849 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 - - Familial, autosomal dominant - - - - - Johan den Dunnen 00057161
0000043852 see paper; ... - - Familial, autosomal dominant - - - - - Johan den Dunnen 00056460
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