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783554002: Autosomal recessive limb girdle muscular dystrophy type 2U (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3759328019 Autosomal recessive limb girdle muscular dystrophy type 2U en Synonym Active Only initial character case insensitive SNOMED CT core module
3759329010 Autosomal recessive limb girdle muscular dystrophy type 2U (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3759330017 Autosomal recessive limb girdle muscular dystrophy due to ISPD deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3759331018 LGMD2U - autosomal recessive limb girdle muscular dystrophy type 2U en Synonym Active Entire term case sensitive 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 2U Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2U Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Existential restriction modifier
Autosomal recessive limb girdle muscular dystrophy type 2U Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2U Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal recessive limb girdle muscular dystrophy type 2U 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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