Phenotypes for disease #03811 (SPG56 (paraplegia, spastic, type 56, autosomal recessive (SPG-56)), OMIM:615030)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000060448 Spastic paraplegia 56, autosomal recessive (OMIM:615030) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080879
0000104229 - - - Unknown - - - - - Isabelle Coupry 00131878
0000337245 Abnormality of movement, Spastic paraparesis, Unsteady gait - - Familial, autosomal recessive 02y - - - - Andreas Laner 00448056
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