Phenotypes for disease #00195 (HMN5A (neuropathy, motor, distal, hereditary, type Va (HMN-5A)), OMIM:600794)

22 entries on 1 page. Showing entries 1 - 22.
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Phenotype details     

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Diagnosis/Definite     

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Age/Onset     

Age/Examination     

Age/Diagnosis     

Protein     

Phenotype/Onset     

Owner     

Individual ID     
0000001695 hereditary motor neuropathy, distal (dHMN) - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002781
0000001696 hereditary motor neuropathy, distal (dHMN) - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002782
0000001697 hereditary motor neuropathy, distal (dHMN) - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002783
0000001698 hereditary motor neuropathy, distal (dHMN) - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002784
0000001699 hereditary motor neuropathy, distal (dHMN) - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002785
0000001700 hereditary motor neuropathy, distal (dHMN) - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002786
0000001701 hereditary motor neuropathy, distal (dHMN) - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002787
0000001702 hereditary motor neuropathy, distal (dHMN) - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002788
0000001703 hereditary motor neuropathy, distal (dHMN) - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002789
0000001716 hereditary motor neuropathy, distal (dHMN) - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002802
0000001717 hereditary motor neuropathy, distal (dHMN) - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002803
0000001750 perypheral neuropathy (PNP); sensory-motor PNP with pyramidal signs - - Unknown - - - - - María-Jesús Sobrido 00002836
0000001758 CMT2; CMT with and without pyramidal signs - - Familial - - - - - María-Jesús Sobrido 00002844
0000001769 HMN II, dHMN - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002855
0000001772 Hereditary spastic paraparesis and primary lateral sclerosis - - Unknown - - - - - María-Jesús Sobrido 00002858
0000001773 dHMN - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002859
0000001775 dHMN - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002861
0000001776 - - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002862
0000001777 - - - Familial, autosomal dominant - - - - - María-Jesús Sobrido 00002863
0000001813 CMT2/dHMN and piramidal signs - - Unknown - - - - - María-Jesús Sobrido 00002899
0000001821 Progressive spastic motor deficit, reactive gliosis in the spinal cord & neurogenic muscular atrophy; - - Unknown - - - - - María-Jesús Sobrido 00002907
0000292365 Demyelinating peripheral neuropathy (HP:0007108), decreased nerve conduction velocity (HP:0000762), pes cavus (HP:0001761) CMT - Unknown 42y 48y - - Demyelinating peripheral neuropathy (HP:0007108), decreased nerve conduction velocity (HP:0000762), pes cavus (HP:0001761) Yvet den Hartog 00399254
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