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


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Only initial character case insensitive (core metadata concept) SNOMED CT core
3437355017 Autosomal recessive limb girdle muscular dystrophy type 2J en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3437356016 Limb-girdle muscular dystrophy 2J titin gene mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) 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 (disorder) Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) Finding site Skeletal muscle structure true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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