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multisystemisk
multisystemic

fabry sygdom er en nedarvet heterogen og multisystemisk progressiv sygdom, der rammer både mænd og kvinder.
fabry disease is an inherited heterogeneous and multisystemic progressive disease, that affects both males and females.

neonatal multisystemisk inflammatorisk sygdom (nomid) / kronisk infantilt neurologisk hud- og ledsyndrom (cinca)
neonatal-onset multisystem inflammatory disease (nomid) / chronic infantile neurological, cutaneous, articular syndrome (cinca)

mps vi er en heterogen og multisystemisk lidelse, karakteriseret ved mangel på n-acetylgalactoasamine 4-sulfatase, en lysosomal hydrolase som katalyserer hydrolysen af sulfat-delen af glycosaminoglycan, dermatansulfat.
mps vi is a heterogeneous and multisystemic disorder characterized by the deficiency of n-acetylgalactoasamine 4-sulfatase, a lysosomal hydrolase which catalyses the hydrolysis of sulfate moiety of the glycosaminoglycan, dermatan sulfate.