723406000: Embryopathy caused by mycophenolate mofetil (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Congenital disease\Congenital anomaly\Congenital malformation syndrome\Mycophenolate mofetil embryopathy
• \Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Mycophenolate mofetil embryopathy

Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3424453012	Embryopathy caused by mycophenolate mofetil (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3424454018	Embryopathy caused by mycophenolate mofetil	en	Synonym	Active	Case insensitive	SNOMED CT core
3424455017	Mycophenolate mofetil embryopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
3424456016	A malformative syndrome due to the teratogenic effect of mycophenolate mofetil (MMF), an effective immunosuppressive agent widely used for the prevention of organ rejection after organ transplantation. To date the majority of cases have been offspring of women who received a solid organ transplant. The newborn or fetus generally has external ear anomalies. Cleft lip-palate with micrognathia is frequently observed. Aberrant orofacial cleft has been observed in one case. Ocular anomalies, such as microphthalmia and iris or chorioretinal coloboma are also frequent. Distal limbs anomalies as well as congenital malformations of the heart, kidneys and/or central nervous system may also be observed.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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