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


Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3705802011 Autosomal dominant limb-girdle muscular dystrophy type 1H en Synonym Active Initial character case insensitive SNOMED CT core
3705803018 Autosomal dominant limb-girdle muscular dystrophy type 1H (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3705804012 A subtype of autosomal dominant limb-girdle muscular dystrophy with characteristics of slowly progressive proximal muscular weakness initially affecting the lower limbs (and later involving the upper limbs), hypotrophy of upper and lower limb-girdle muscles, hyporeflexia, calf hypertrophy, and increased serum creatine kinase. There is no involvement of oculo-facial-bulbar muscles and cardiac muscle. 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 1H Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal dominant limb-girdle muscular dystrophy type 1H Clinical course Progressive true Inferred relationship Some 2
Autosomal dominant limb-girdle muscular dystrophy type 1H Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal dominant limb-girdle muscular dystrophy type 1H Is a Autosomal dominant muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal dominant limb-girdle muscular dystrophy type 1H Finding site Skeletal muscle structure true Inferred relationship Some 1

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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