Phenotypes for disease #01109 (MDDGC2;LGMDR14;LGMD2N (dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C2 (LGMDR14, LGMD2N)), OMIM:613158)

1 entry on 1 page. Showing entry 1.
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     
0000257313 Muscle weakness HP:0001324 Hypotonia HP:0001252 - - Familial, autosomal recessive - - - - - Ibrahim Sahin 00361915
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.