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718180000: Autosomal recessive limb girdle muscular dystrophy type 2I (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
3311396016 Autosomal recessive limb girdle muscular dystrophy type 2I (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3311397013 Autosomal recessive limb girdle muscular dystrophy type 2I en Synonym Active Only initial character case insensitive SNOMED CT core module
3311398015 Limb girdle muscular dystrophy due to deficiency of fukutin related protein 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 2I Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Existential restriction modifier
Autosomal recessive limb girdle muscular dystrophy type 2I Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2I Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2I Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2I 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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