Phenotypes for disease #05035 (SCA-21 (ataxia, spinocerebellar, type 21 (SCA-21)), OMIM:607454)

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     
0000129434 - spinocerebellar ataxia SCAR-21 Familial, autosomal recessive 02y06m 00y10m - - - Lior Cohen 00164324
0000258850 (+) Muscular hypotonia,(+) Motor delay,(+) Joint hypermobility,(+) Quadriceps muscle weakness,(+) Chronic constipation 03y - Unknown - - - - - Andreas Laner 00363500
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