Disease #02181 (RBMX-1B (myopathy, reducing body, X-linked, type 1b (RBMX-1B)), OMIM:300718)

Official abbreviation RBMX-1B
Name myopathy, reducing body, X-linked, type 1b (RBMX-1B)
OMIM ID 300718
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FHL1
Associated tissues -
Disease features -
Remarks -