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726618007: Autosomal recessive limb girdle muscular dystrophy type 2M (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3451016013 Autosomal recessive limb girdle muscular dystrophy type 2M (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3451017016 Autosomal recessive limb girdle muscular dystrophy type 2M 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 2M Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Existential restriction modifier
Autosomal recessive limb girdle muscular dystrophy type 2M Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2M Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2M Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2M 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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