Phenotypes for disease #04043 (SPG57 (paraplegia, spastic, type 57, autosomal recessive (SPG-57)), OMIM:615658)

7 entries on 1 page. Showing entries 1 - 7.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000045740 spastic paraplegia, cognitive impairment - - Familial, autosomal recessive 08y - 01y? - - Mahmoud Koko 00059235
0000054325 - - - Familial, autosomal recessive - - - - - Christian Beetz 00074500
0000054326 subclinical signs for upper motoneuron pathology - - Familial, autosomal dominant 26y - - - - Christian Beetz 00074496
0000054327 - - - Familial, autosomal recessive - - - - - Christian Beetz 00074498
0000054328 - - - Familial, autosomal recessive - - - - - Christian Beetz 00074499
0000054329 - - - Unknown - - - - - Christian Beetz 00074502
0000054330 - - - Unknown - - - - - Christian Beetz 00074503
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.