EMDN Rehberi | UTSBridge

MONOGENETIC DISORDERS

Sub groups

Code	Official name	Devices
W0106010101	CYSTIC FIBROSISNo sub groups	23
W0106010102	DUCHENNE MUSCULAR DYSTROPHYNo sub groups	2
W0106010103	FACTOR V LEIDENNo sub groups	24
W0106010104	FRAGILE X SYNDROMENo sub groups	10
W0106010105	HAEMOCHROMATOSISNo sub groups	14
W0106010106	HAEMOPHILIANo sub groups	No registered devices in this group.
W0106010107	HUNTINGTON CHOREANo sub groups	2
W0106010108	POLYCYSTIC KIDNEY DISEASENo sub groups	5
W0106010109	SICKLE CELL ANEMIANo sub groups	7
W0106010110	TAY SACHS DISEASENo sub groups	No registered devices in this group.
W0106010111	THALASSAEMIANo sub groups	23
W0106010112	FRIEDREICH'S ATAXIANo sub groups	1
W0106010113	SPINOCEREBELLAR ATAXINS TYPE 1,2,3,6,7,8No sub groups	1
W0106010114	PROTHROMBIN MUTATIONNo sub groups	18
W0106010115	COMBINED FACTOR II / FACTOR V LEIDENNo sub groups	11
W0106010116	OTHER THROMBOPHILIA MUTATIONS (PROC, PROS1, MTHFR, SERPINC1, SEPINE1, F11, F12, F13, OTHER F2/F5)No sub groups	30
W0106010117	OTHER HEMOPHILIA MUTATIONS (VWF, F8, F9)No sub groups	1
W0106010118	MYOTONIC DYSTROPHY TYPE 1 OR STEINERT'S DISEASENo sub groups	1
W0106010199	MONOGENETIC DISORDERS TESTS - OTHERNo sub groups	139