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771334000: Autosomal dominant limb-girdle muscular dystrophy type 1H (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3705802011 Autosomal dominant limb-girdle muscular dystrophy type 1H en Synonym Active Only initial character case insensitive SNOMED CT core module
3705803018 Autosomal dominant limb-girdle muscular dystrophy type 1H (disorder) en Fully specified name 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 dominant limb-girdle muscular dystrophy type 1H Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb-girdle muscular dystrophy type 1H Is a Autosomal dominant muscular dystrophy with limb girdle distribution true Inferred relationship Existential restriction modifier
Autosomal dominant limb-girdle muscular dystrophy type 1H Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb-girdle muscular dystrophy type 1H Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb-girdle muscular dystrophy type 1H 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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