Phenotypes for disease #02755 (MSMA (myopathy, myosin storage, autosomal dominant (MSMA)), OMIM:608358)

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000257390 Hypotonia HP:0001252 - - Isolated (sporadic) - - - - - Ibrahim Sahin 00361997
0000357016 Muscular dystrophy LGMD CMYO7A Isolated (sporadic) - - - - - Camille Verebi 00472207
Legend   How to query  


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.