Phenotypes for disease #02078 (SPG5A (paraplegia, spastic, autosomal recessive, type 5A (SPG-5A)), OMIM:270800)

5 entries on 1 page. Showing entries 1 - 5.
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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     
0000029694 - - - Familial, autosomal recessive - - - - - David Lynch 00039358
0000029699 - - - Familial, autosomal recessive - - - - - David Lynch 00039359
0000035827 - - - Unknown - - - - - Johan den Dunnen 00046994
0000035828 - - - Unknown - - - - - Johan den Dunnen 00046995
0000296576 Mental Retardation Progressive spastic paraparesis HSP SPG5A Familial, autosomal recessive 22y 15y 11y - - Sherifa Ahmed Hamed 00403911
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