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MIM:300717 - REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET; RBMX1A
Xenbase Genes: fhl1
Human Disease Resource: OMIM
MONDO:0010414 - myopathy, reducing body, X-linked, early-onset, severe |
MONDO:0019948 - reducing body myopathy |
DOID:0080090 - reducing body myopathy 1A |