UDI CompassMONOGENETIC DISORDERS
EMDN W01060101
Parent W010601 INBORN GENE OR CHROMOSOME ALTERATIONS
Registry term list. Not a clinical opinion. 0 devices carry this code.
Devices
No devices in this snapshot carry this code.
EMDN W01060101
Parent W010601 INBORN GENE OR CHROMOSOME ALTERATIONS
Registry term list. Not a clinical opinion. 0 devices carry this code.
No devices in this snapshot carry this code.