All diseases

OMIM ID
602771
OMIM term:
RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
Alternative terms:
RIGID SPINE SYNDROME; RSS
MYOPATHY, SEPN1-RELATED
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE, WITH EARLY SPINE RIGIDITY; MDRS1
MULTICORE MYOPATHY, SEVERE CLASSIC FORM
MINICORE MYOPATHY, SEVERE CLASSIC FORM
MULTIMINICORE DISEASE, SEVERE CLASSIC FORM
DESMIN-RELATED MYOPATHY WITH MALLORY BODIES
MUSCULAR DYSTROPHY, CONGENITAL, EICHSFELD TYPE
(∗) Location:
1p36.11  
(†) Associated OMIM genes:
SEPN1  
(‡) Associated MGI genes:
Sepn1  

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