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715340002: Autosomal recessive limb girdle muscular dystrophy type 2D (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3302268016 Alpha-sarcoglycanopathy LGMD2D (limb girdle muscular dystrophy type 2D) en Synonym Active Only initial character case insensitive SNOMED CT core module
3302279014 Autosomal recessive limb girdle muscular dystrophy type 2D (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3302280012 Autosomal recessive limb girdle muscular dystrophy type 2D 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 recessive limb girdle muscular dystrophy type 2D Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Existential restriction modifier
Autosomal recessive limb girdle muscular dystrophy type 2D Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2D Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2D Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2D 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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