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Summary Literature (0)
MIM:300718 - REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET; RBMX1B

Xenbase Genes: fhl1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010415 - myopathy, reducing body, X-linked, childhood-onset
MONDO:0019948 - reducing body myopathy

Disease Ontology (DO):
DOID:0080090 - reducing body myopathy 1A
DOID:0080687 - reducing body myopathy 1B