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116022009: Multiple congenital malformations (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    178533010 Multiple congenital malformations en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    674195014 Multiple congenital malformations (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    178533010 Multiple congenital malformations en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    178533010 Multiple congenital malformations en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    674195014 Multiple congenital malformations (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    674195014 Multiple congenital malformations (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
    Multiple congenital malformations Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
    Multiple congenital malformations Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Multiple congenital malformations Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Malformation defect spectrum Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Malformation association Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Malformation sequence Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Klippel's disease Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Osteochondrodysplasia with osteopetrosis (disorder) Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Multiple system malformation syndrome Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance (disorder) Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Biemond's syndrome Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    VATER association Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Ullrich-Feichtiger syndrome, chimera Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    schistosomus reflexus Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Cardio-acral-facial syndrome (disorder) Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Cardio-facio-cutaneous syndrome (disorder) Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Bitemporal scars with abnormal eyelashes Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Cleft palate lateral synechia syndrome (disorder) Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Facial milia, lobate tongue, lingual and labial frenula syndrome (disorder) Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    Acrocephalosyndactyly Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)
    A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies). Is a False Multiple congenital malformations Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

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

    Description inactivation indicator reference set

    GB English

    US English

    SAME AS association reference set (foundation metadata concept)

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