Phenotypes for disease #00217 (SPG8 (paraplegia, spastic, autosomal dominant, type 8 (SPG-8)), OMIM:603563)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000001868 hereditary spastic paraplegia hereditary spastic paraplegia SPG8 Familial, autosomal dominant - - 15y - - Marcel Nelen 00003017
0000258853 spastic paraparesis - - Unknown - 61y - - - Andreas Laner 00363503
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