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116022009: Multiple congenital malformations (disorder)

    Status: retired, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    178533010 Multiple congenital malformations en Synonym Active Case insensitive SNOMED CT core
    674195014 Multiple congenital malformations (disorder) en Fully specified name Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Multiple congenital malformations Associated morphology Congenital malformation false Inferred relationship Some
    Multiple congenital malformations Occurrence Congenital false Inferred relationship Some
    Multiple congenital malformations Is a Congenital anomaly false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Schistosomus reflexus Is a False Multiple congenital malformations Inferred relationship Some
    Klippel's disease Is a False Multiple congenital malformations Inferred relationship Some
    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
    Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma Is a False Multiple congenital malformations Inferred relationship Some
    Cardio-acral-facial syndrome Is a False Multiple congenital malformations Inferred relationship Some
    Cardio-facio-cutaneous syndrome 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 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, chimaera Is a False Multiple congenital malformations Inferred relationship Some
    Acrocephalosyndactyly Is a False Multiple congenital malformations Inferred relationship Some
    Oromandibular-limb hypogenesis spectrum Is a False Multiple congenital malformations Inferred relationship Some

    Reference Sets

    Australian dialect reference set

    Concept inactivation indicator reference set

    SAME AS association reference set

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