FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

719986000: dystrophie musculaire des ceintures autosomique dominante type 1C (trouble)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3318720013 Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3318721012 Autosomal dominant limb girdle muscular dystrophy type 1C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    3318722017 Limb girdle muscular dystrophy due to caveolin-3 deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3318723010 Limb-girdle muscular dystrophy 1C caveolin myopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    755131000241112 dystrophie musculaire des ceintures autosomique dominante type 1C (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
    967501000172111 dystrophie musculaire des ceintures autosomique dominante type 1C fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
    990361000172117 dystrophie musculaire des ceintures par déficit en cavéoline-3 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
    3318724016 A limb girdle muscular dystrophy caused by caveolin-3 deficiency with characteristics of weakness in limb-girdle muscles, calf muscle hypertrophy and lack of respiratory and cardiac involvement. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 1
    Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 1
    Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) évolution clinique (attribut) progressif false Inferred relationship Some 2
    Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) est un(e) (attribut) Autosomal dominant muscular dystrophy with limb girdle distribution false Inferred relationship Some
    Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 2
    Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 3
    Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
    Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) survenue (attribut) congénital false Inferred relationship Some 2
    Autosomal dominant limb girdle muscular dystrophy type 1C (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 3
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

    Back to Start