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Summary Literature (0)
MIM:300717 - REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET; RBMX1A

Xenbase Genes: fhl1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010414 - omental fat pad
MONDO:0019948 - reducing body myopathy

Disease Ontology (DO):
DOID:0080090 - reducing body myopathy 1A