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1279884000: Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5234336010 Limb girdle muscular dystrophy type R24 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5234337018 Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5234338011 POMGNT2-related limb girdle muscular dystrophy R24 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5234339015 POMGNT2-related muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5234340018 Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5234341019 A rare autosomal recessive limb girdle muscular dystrophy with characteristics of infantile to adolescent onset of a milder form of limb-girdle muscular dystrophy with or without intellectual disability. Patients present variable proximal limb muscular weakness with calf hypertrophy and elevated serum creatine kinase. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5896061000052119 POMGNT2-relaterad muskeldystrofi i skulder-bäckengördel, typ R24 sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24 (disorder) Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Some
Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24 (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 2
Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24 (disorder) Finding site Skeletal muscle structure true Inferred relationship Some 1
Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24 (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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