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720523006: Autosomal recessive limb girdle muscular dystrophy type 2K (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
3321128016 Autosomal recessive limb girdle muscular dystrophy type 2K (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3321129012 Autosomal recessive limb girdle muscular dystrophy type 2K en Synonym Active Only initial character case insensitive SNOMED CT core module
3321130019 Limb girdle muscular dystrophy with intellectual disability syndrome 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 2K Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Existential restriction modifier
Autosomal recessive limb girdle muscular dystrophy type 2K Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2K Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2K Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2K 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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