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783554002: Autosomal recessive limb girdle muscular dystrophy type 2U (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3759328019 Autosomal recessive limb girdle muscular dystrophy type 2U en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3759329010 Autosomal recessive limb girdle muscular dystrophy type 2U (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3759330017 Autosomal recessive limb girdle muscular dystrophy due to ISPD deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3759331018 LGMD2U - autosomal recessive limb girdle muscular dystrophy type 2U en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759332013 A rare subtype of autosomal recessive limb-girdle muscular dystrophy disorder with characteristics of infantile to childhood-onset of slowly progressive, principally proximal shoulder and/or pelvic-girdle muscular weakness that typically presents with positive Gowers' sign and is associated with elevated creatine kinase levels, hyporeflexia, joint and achilles tendon contractures and muscle hypertrophy usually of the thighs, calves and/or tongue. Other highly variable features include cerebellar, cardiac and ocular abnormalities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759328019 Autosomal recessive limb girdle muscular dystrophy type 2U en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3759329010 Autosomal recessive limb girdle muscular dystrophy type 2U (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3759330017 Autosomal recessive limb girdle muscular dystrophy due to ISPD deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3759331018 LGMD2U - autosomal recessive limb girdle muscular dystrophy type 2U en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759332013 A rare subtype of autosomal recessive limb-girdle muscular dystrophy disorder with characteristics of infantile to childhood-onset of slowly progressive, principally proximal shoulder and/or pelvic-girdle muscular weakness that typically presents with positive Gowers' sign and is associated with elevated creatine kinase levels, hyporeflexia, joint and achilles tendon contractures and muscle hypertrophy usually of the thighs, calves and/or tongue. Other highly variable features include cerebellar, cardiac and ocular abnormalities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3446381001000112 ISPD-assoziierte Gliedergürtelmuskeldystrophie R20 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5591661000241118 dystrophie musculaire des ceintures autosomique récessive de type 2U fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5591661000241118 dystrophie musculaire des ceintures autosomique récessive de type 2U fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3446381001000112 ISPD-assoziierte Gliedergürtelmuskeldystrophie R20 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive limb girdle muscular dystrophy type 2U Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2U Is a Autosomal recessive muscular dystrophy with limb girdle distribution (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive limb girdle muscular dystrophy type 2U Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2U Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2U Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

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