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

732931006: Autosomal recessive limb girdle muscular dystrophy type 2R (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    3467549016 Autosomal recessive limb girdle muscular dystrophy type 2R (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
    3467550016 Autosomal recessive limb girdle muscular dystrophy type 2R en Synonym Active Only initial character case insensitive SNOMED CT core module
    3467551017 Autosomal recessive limb girdle muscular dystrophy due to desmin deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Autosomal recessive limb girdle muscular dystrophy type 2R Is a Autosomal recessive muscular dystrophy with limb girdle distribution false Inferred relationship Existential restriction modifier
    Autosomal recessive limb girdle muscular dystrophy type 2R Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 1
    Autosomal recessive limb girdle muscular dystrophy type 2R Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
    Autosomal recessive limb girdle muscular dystrophy type 2R Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Autosomal recessive limb girdle muscular dystrophy type 2R Clinical course Progressive false Inferred relationship Existential restriction modifier 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start