Phenotypes for disease #00213 (SPG10 (paraplegia, spastic, autosomal dominant, type 10 (SPG-10)), OMIM:604187)

7 entries on 1 page. Showing entries 1 - 7.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000001860 hereditary spastic paraplegia hereditary spastic paraplegia - Familial, autosomal dominant - - <00y03m - - Marcel Nelen 00003009
0000001861 hereditary spastic paraplegia hereditary spastic paraplegia SPG10 Familial, autosomal dominant - - 29y - - Marcel Nelen 00003010
0000001862 hereditary spastic paraplegia hereditary spastic paraplegia - Familial, autosomal dominant - - 47y - - Marcel Nelen 00003011
0000029695 - - - Familial, autosomal dominant - - - - - David Lynch 00039353
0000029696 - - - Familial, autosomal dominant - - - - - David Lynch 00039354
0000243164 Lower limb spasticity, Spastic paraparesis, Spastic gait, Decreased vibratory sense in the lower limbs - - Unknown 60y - - - - Andreas Laner 00324664
0000291834 Peripheral neuropathy (HP:0009830), Spastic paraplegia (HP:0001258), No decreased nerve conduction velocity (-HP:0000762) CMT SPG10 Familial, autosomal dominant 60y - 40y Peripheral neuropathy (HP:0009830), Spastic paraplegia (HP:0001258), No decreased nerve conduction velocity (-HP:0000762) - Yvet den Hartog 00398668
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