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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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Multiple congenital malformations Is a Congenital malformation false Inferred relationship Some
    Multiple congenital malformations Occurrence Congenital false Inferred relationship Some
    Multiple congenital malformations Associated morphology Congenital malformation false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Malformation defect spectrum Is a False Multiple congenital malformations Inferred relationship Some
    Malformation association Is a False Multiple congenital malformations Inferred relationship Some
    Malformation sequence Is a False Multiple congenital malformations Inferred relationship Some
    Klippel's disease Is a False Multiple congenital malformations Inferred relationship Some
    Osteochondrodysplasia with osteopetrosis Is a False Multiple congenital malformations Inferred relationship Some
    Multiple system malformation syndrome Is a False Multiple congenital malformations Inferred relationship Some
    Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance Is a False Multiple congenital malformations Inferred relationship Some
    Biemond's syndrome Is a False Multiple congenital malformations Inferred relationship Some
    VATER association Is a False Multiple congenital malformations Inferred relationship Some
    Ullrich-Feichtiger syndrome, chimera Is a False Multiple congenital malformations Inferred relationship Some
    schistosomus reflexus Is a False Multiple congenital malformations Inferred relationship Some
    Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a False Multiple congenital malformations Inferred relationship Some
    Cardio-acral-facial syndrome (disorder) Is a False Multiple congenital malformations Inferred relationship Some
    Cardio-facio-cutaneous syndrome (disorder) Is a False Multiple congenital malformations Inferred relationship Some
    Bitemporal scars with abnormal eyelashes Is a False Multiple congenital malformations Inferred relationship Some
    Cleft palate lateral synechia syndrome Is a False Multiple congenital malformations Inferred relationship Some
    Facial milia, lobate tongue, lingual and labial frenula syndrome (disorder) Is a False Multiple congenital malformations Inferred relationship Some
    Acrocephalosyndactyly Is a False Multiple congenital malformations Inferred relationship Some
    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 Some

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    SAME AS association reference set (foundation metadata concept)

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