Disease #02180 (RBMX1A (myopathy, reducing body, X-linked, type 1a (RBMX-1A)), OMIM:300717)

Official abbreviation RBMX1A
Name myopathy, reducing body, X-linked, type 1a (RBMX-1A)
OMIM ID 300717
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FHL1
Associated tissues -
Disease features -
Remarks X-linked dominant, severe, infantile or early childhood onset