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719989007: Autosomal dominant limb girdle muscular dystrophy type 1F (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
3318731017 Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3318732012 Autosomal dominant limb girdle muscular dystrophy type 1F 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 dominant limb girdle muscular dystrophy type 1F Is a Autosomal dominant muscular dystrophy with limb girdle distribution true Inferred relationship Existential restriction modifier
Autosomal dominant limb girdle muscular dystrophy type 1F Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1F Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 3
Autosomal dominant limb girdle muscular dystrophy type 1F Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1F Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1F Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 3
Autosomal dominant limb girdle muscular dystrophy type 1F Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb girdle muscular dystrophy type 1F Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb girdle muscular dystrophy type 1F Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb girdle muscular dystrophy type 1F 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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