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719989007: Autosomal dominant limb girdle muscular dystrophy type 1F (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3318731017 Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3318732012 Autosomal dominant limb girdle muscular dystrophy type 1F en Synonym Active Initial character case insensitive SNOMED CT core
3318733019 A form of limb girdle muscular dystrophy with characteristics of muscle weakness affecting the pelvic girdle and especially the iliopsoas muscle. Respiratory impairment may be observed in advanced stages. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant limb girdle muscular dystrophy type 1F Finding site Skeletal muscle structure true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1F Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1F Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1F Clinical course Progressive true Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1F Is a Autosomal dominant muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal dominant limb girdle muscular dystrophy type 1F Finding site Skeletal muscle structure false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1F Finding site Skeletal muscle structure false Inferred relationship Some 3
Autosomal dominant limb girdle muscular dystrophy type 1F Associated morphology Developmental abnormality false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1F Occurrence Congenital false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1F Associated morphology Dystrophy false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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