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

8 entries on 1 page. Showing entries 1 - 8.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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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
0000357698 Gait disturbance since birth; mother and brother also affected. Required orthopedic shoes as a child; unable to run. Worsening gait for over 10 years, with increased clumsiness in the right leg. Denies sensory disturbances. Gait disturbance Spastic paraplegia 10, autosomal dominant Familial, autosomal dominant 36? 46y 05y Chilhood onset - Maria Elena García Paya 00472903
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