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719987009: Autosomal dominant limb girdle muscular dystrophy type 1D (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3318725015 Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3318726019 Autosomal dominant limb girdle muscular dystrophy type 1D en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant limb girdle muscular dystrophy type 1D Is a Autosomal dominant muscular dystrophy with limb girdle distribution true Inferred relationship Existential restriction modifier
Autosomal dominant limb girdle muscular dystrophy type 1D Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1D Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 3
Autosomal dominant limb girdle muscular dystrophy type 1D Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1D Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1D Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 3
Autosomal dominant limb girdle muscular dystrophy type 1D Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb girdle muscular dystrophy type 1D Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb girdle muscular dystrophy type 1D Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb girdle muscular dystrophy type 1D Clinical course Progressive true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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