Phenotypes for disease #01458 (DM1 (dystrophy, myotonic, type 1 (DM-1, Steinert disease)), OMIM:160900)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000350543 - - - Familial, autosomal dominant - - - - - Hilde Swinkels 00464544
0000350606 - - - Familial, autosomal dominant - - - - - Hilde Swinkels 00464529
0000350608 - - - Familial, autosomal dominant - - - - - Hilde Swinkels 00464618
0000350610 - - - Familial, autosomal dominant - - - - - Hilde Swinkels 00464619
0000350611 - - - Familial, autosomal dominant - - - - - Hilde Swinkels 00464620
0000350612 - - - Familial, autosomal dominant - - - - - Hilde Swinkels 00464621
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