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Summary Literature (0)
MIM:602771 - CONGENITAL MYOPATHY 3 WITH RIGID SPINE; CMYP3

Xenbase Genes: selenon

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011271 - rigid spine muscular dystrophy 1
MONDO:0017939 - classic multiminicore myopathy
MONDO:0018948 - multiminicore myopathy
MONDO:0019398 - desmin-related myopathy with Mallory body-like inclusions
MONDO:0019951 - rigid spine syndrome

Disease Ontology (DO):
DOID:0110633 - rigid spine muscular dystrophy 1