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723406000: embryopathie door mycofenolaatmofetil (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
3424454018 Embryopathy caused by mycophenolate mofetil en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424455017 Mycophenolate mofetil embryopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6630401000146114 embryopathie door mycofenolaatmofetil (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6630411000146111 embryopathie door mycofenolaatmofetil nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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 Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Embryopathy caused by mycophenolate mofetil (disorder) Is a aandoening bij drug of geneesmiddel (aandoening) false Inferred relationship Some
Embryopathy caused by mycophenolate mofetil (disorder) Is a Congenital malformation syndrome due to known exogenous cause false Inferred relationship Some
Embryopathy caused by mycophenolate mofetil (disorder) Is a Disorder of fetal structure false Inferred relationship Some
Embryopathy caused by mycophenolate mofetil (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 1
Embryopathy caused by mycophenolate mofetil (disorder) Causative agent Mycophenolate mofetil (substance) true Inferred relationship Some 1
Embryopathy caused by mycophenolate mofetil (disorder) Occurrence Congenital true Inferred relationship Some 1
Embryopathy caused by mycophenolate mofetil (disorder) Finding site Fetal structure true Inferred relationship Some 1
Embryopathy caused by mycophenolate mofetil (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Embryopathy caused by mycophenolate mofetil (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Embryopathy caused by mycophenolate mofetil (disorder) Is a Congenital malformation syndrome (disorder) true Inferred relationship Some
Embryopathy caused by mycophenolate mofetil (disorder) Is a aandoening ingedeeld naar anatomische of verworven lichaamsstructuur (aandoening) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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