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725042001: Autosomal recessive limb girdle muscular dystrophy type 2J (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3437354018 Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3437355017 Autosomal recessive limb girdle muscular dystrophy type 2J en Synonym Active Initial character case insensitive SNOMED CT core
3437356016 Limb-girdle muscular dystrophy 2J titin gene mutation en Synonym Active Initial character case insensitive SNOMED CT core
3437357013 A form of limb-girdle muscular dystrophy that usually has a childhood onset (but can range from the first to third decade of life) of severe progressive proximal weakness, eventually involving the distal muscles. Some patients may remain ambulatory but most are wheelchair dependant 20 years after onset. Caused by homozygous mutation in the titin gene (TTN). en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive limb girdle muscular dystrophy type 2J Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2J Clinical course Progressive true Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2J Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal recessive limb girdle muscular dystrophy type 2J Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2J 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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