Phenotypes for disease #00811 (SMALED1 (atrophy, muscular, spinal, lower extremity predominant, type 1), OMIM:158600)

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     
0000295490 Myopathy, Exercise intolerance, Myopathic facies, Pectoralis amyotrophy, Shoulder girdle muscle weakness, Upper limb muscle weakness, Muscular dystrophy 6y - Isolated (sporadic) 18y - - - - Andreas Laner 00402727
0000351389 Neurodevelopmental delay, Gait ataxia, Hypotonia, Elevated circulating hepatic transaminase concentration - - Isolated (sporadic) 04y - - - - Andreas Laner 00466002
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