Phenotypes for disease #05116 (MDDGB (dystrophy, muscular, dystroglycanopathy, type B (MDDGB)))

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000043176 dystroglycanopathy - - Unknown - - - - - Tom Winder 00056488
0000043177 dystroglycanopathy - - Unknown - - - - - Tom Winder 00056489
0000043178 dystroglycanopathy - - Unknown - - - - - Tom Winder 00056490
0000043179 dystroglycanopathy - - Unknown - - - - - Tom Winder 00056491
0000043180 dystroglycanopathy - - Unknown - - - - - Tom Winder 00056492
0000043181 dystroglycanopathy - - Unknown - - - - - Tom Winder 00056493
0000043183 see paper; II2 frequent cramps, enlarged calves, behavioural problems, ...; II3 hyperCK, cramps from age 6, enlarged calves., right bundle branch block, ... - - Isolated (sporadic) - - - proximal limb weakness; proximal limb weakness - Johan den Dunnen 00056495
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