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725907002: Autosomal recessive limb girdle muscular dystrophy type 2Y (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3446315013 Autosomal recessive limb girdle muscular dystrophy type 2Y (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3446316014 Autosomal recessive limb girdle muscular dystrophy type 2Y en Synonym Active Initial character case insensitive SNOMED CT core
3446317017 Autosomal recessive muscular dystrophy due to LAP1B (lamin-associated protein 1B) deficiency en Synonym Active Initial character case insensitive SNOMED CT core
3446318010 Autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency en Synonym Active Initial character case insensitive SNOMED CT core
3446319019 Muscular dystrophy with progressive weakness, distal contracture and rigid spine en Synonym Active Case insensitive SNOMED CT core
3446320013 A form of limb-girdle muscular dystrophy presenting in the first or second decades of life with characteristics of slowly progressive proximal and distal muscle weakness and atrophy. Additional manifestations include contractures of the proximal and distal interphalangeal hand joints, rigid spine, restricted pulmonary function and mild cardiomyopathy. 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 2Y Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2Y Clinical course Progressive true Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2Y Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal recessive limb girdle muscular dystrophy type 2Y Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2Y 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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