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254245008: Congenital malformation syndrome due to known exogenous cause (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    378475012 Congenital malformation syndrome due to known exogenous cause en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    645109012 Congenital malformation syndrome due to known exogenous cause (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    378475012 Congenital malformation syndrome due to known exogenous cause en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    378475012 Congenital malformation syndrome due to known exogenous cause en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    645109012 Congenital malformation syndrome due to known exogenous cause (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    645109012 Congenital malformation syndrome due to known exogenous cause (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital malformation syndrome due to known exogenous cause Is a Congenital malformation syndromes due to known exogenous causes false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital malformation syndrome due to known exogenous cause Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital malformation syndrome due to known exogenous cause Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital malformation syndrome due to known exogenous cause Is a Congenital malformation syndrome false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital malformation syndrome due to known exogenous cause Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital malformation syndrome due to known exogenous cause Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    [X]Other congenital malformation syndromes due to known exogenous causes Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital malformation caused by cytotoxic agents (disorder) Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal benzodiazepine syndrome Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal captopril/enalapril syndrome Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal carbamazepine syndrome Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Foetal cocaine syndrome Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal minoxidil syndrome (disorder) Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal misoprostol syndrome Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal primidone syndrome Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal toluene syndrome Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal valproate syndrome (disorder) Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Thalidomide embryopathy syndrome Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    embryopathie causée par l'acide rétinoïque Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal warfarin syndrome Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal methyl mercury syndrome (disorder) Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal trimethadione syndrome (disorder) Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal hydantoin syndrome Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    fœtus ou nouveau-né affecté par l'usage maternel d'alcool Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    fœtus ou nouveau-né affecté par le transfert placentaire ou mammaire d'alcool Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Embryopathy caused by phenobarbital (disorder) Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Embryofetopathy caused by indomethacin (disorder) Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Fetal iodine syndrome refers to symptoms and signs that may be observed in a fetus or newborn when the mother was exposed during pregnancy to inappropriate (insufficient or excessive) amounts of iodine. Iodine deficiency is associated with goitre and hypothyroidism. When severe iodine deficiency occurs during pregnancy, it is associated with congenital hypothyroidism that is manifested by increased neonatal morbi-mortality and severe mental dysfunction, hyperactivity, attention disorders and a substantial decrease of IQ of an irreversible nature. Excessive iodine ingestion during the third trimester of pregnancy can result in hypothyroidism and fetal goitre due to a prolonged inhibition of thyroid hormone synthesis, an increase in thyrotropin (TSH). Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Mycophenolate mofetil (MMF) embryopathy is a malformative syndrome due to the teratogenic effect of MMF, an effective immunosuppressive agent widely used for the prevention of organ rejection after organ transplantation. Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Methimazole embryofetopathy Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)
    Retinoid embryopathy Is a False Congenital malformation syndrome due to known exogenous cause Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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