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23756001: Congenital growth alteration (morphologic abnormality)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    39886016 Congenital growth alteration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    753314011 Congenital growth alteration (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2615301000005113 kongenit vækstændring da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    kongenit vækstændring Is a kongenit anomali false Inferred relationship Some
    kongenit vækstændring Is a dysgenese false Inferred relationship Some
    kongenit vækstændring Is a Growth alteration false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Abnormally short growth Is a False kongenit vækstændring Inferred relationship Some
    Abnormally short and broad growth Is a False kongenit vækstændring Inferred relationship Some
    Congenital incomplete expansion Is a False kongenit vækstændring Inferred relationship Some
    kongenit lille statur Is a False kongenit vækstændring Inferred relationship Some
    kongenit abnorm form Is a False kongenit vækstændring Inferred relationship Some
    kongenit hyperplasi Is a False kongenit vækstændring Inferred relationship Some
    Congenital growth disproportion Is a False kongenit vækstændring Inferred relationship Some
    Kongenit abnormt antal Is a False kongenit vækstændring Inferred relationship Some
    Congenital overexpansion Is a False kongenit vækstændring Inferred relationship Some
    Abnormally long growth Is a False kongenit vækstændring Inferred relationship Some
    Forkortet truncus Associated morphology False kongenit vækstændring Inferred relationship Some
    kongenit hypertrofi Is a False kongenit vækstændring Inferred relationship Some
    Unilateral kongenit macrostomia Associated morphology False kongenit vækstændring Inferred relationship Some 1
    Congenital macrostomia Associated morphology False kongenit vækstændring Inferred relationship Some 1
    Reduction of gigantism of foot Direct morphology False kongenit vækstændring Inferred relationship Some 1
    Reduction of gigantism of foot Direct morphology False kongenit vækstændring Inferred relationship Some 1
    Failure of growth of fetal right cardiac ventricle Associated morphology False kongenit vækstændring Inferred relationship Some 2
    Failure of growth of fetal left cardiac ventricle Associated morphology False kongenit vækstændring Inferred relationship Some 2
    Congenital redundant rectal mucosa Associated morphology False kongenit vækstændring Inferred relationship Some 2
    Congenital thickening of talus Associated morphology False kongenit vækstændring Inferred relationship Some 3
    Congenital thickening of tibia Associated morphology False kongenit vækstændring Inferred relationship Some 3
    Congenital thickening of scapula Associated morphology False kongenit vækstændring Inferred relationship Some 3
    Congenital thickening of tarsal bone Associated morphology False kongenit vækstændring Inferred relationship Some 3
    Congenital thickening of radius Associated morphology False kongenit vækstændring Inferred relationship Some 3
    Congenital redundant rectal mucosa Associated morphology False kongenit vækstændring Inferred relationship Some 1
    Infantile spasms-broad thumbs syndrome is a rare neurologic disorder characterized by profound developmental delay, facial dysmorphism (i.e. microcephaly, large anterior fontanel, hypertelorism, downslanting palpebral fissures, beaked nose, micrognathia), broad thumbs and flexion and/or extension spasms. Bilateral cataracts, hypertrophic cardiomyopathy and hydrocele have also been reported. EEG shows hypsarrhythmic features and MRI may reveal partial agenesis of the corpus callosum, mild brain atrophy and/or ventriculomegaly. There have been no further descriptions in the literature since 1990. Associated morphology False kongenit vækstændring Inferred relationship Some 1

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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