Phenotypes for disease #05554 (CMYO3;RSMD1 (myopathy, congenital, type 3, with rigid spine), OMIM:602771)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000325275 - - Muscular dystrophy, Scoliosis, Scapulohumeral muscular dystrophy, Craniofacial dystonia, 3 of 7 siblings affected Familial, autosomal recessive 24y - - - Andreas Laner 00435032
0000349739 - - Myopathy, Proximal muscle weakness, Gowers sign, Restrictive ventilatory defect Familial, autosomal recessive 22y - 03y - Andreas Laner 00462238
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