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1234819007: Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5084104014 Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5084105010 Limb girdle muscular dystrophy due to POMK deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5084106011 Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5400216018 Limb-girdle muscular dystrophy due to POMK deficiency is a form of limb-girdle muscular dystrophy presenting in infancy with muscle weakness and delayed motor development (eventually learning to walk at 18 months of age) followed by progressive proximal weakness, pseudohypertrophy of calf muscles, mild facial weakness, and borderline intelligence. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5084104014 Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5084105010 Limb girdle muscular dystrophy due to POMK deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5084106011 Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5084107019 A form of limb-girdle muscular dystrophy presenting in infancy with muscle weakness and delayed motor development (eventually learning to walk at 18 months of age) followed by progressive proximal weakness, pseudohypertrophy of calf muscles, mild facial weakness and borderline intelligence. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400216018 Limb-girdle muscular dystrophy due to POMK deficiency is a form of limb-girdle muscular dystrophy presenting in infancy with muscle weakness and delayed motor development (eventually learning to walk at 18 months of age) followed by progressive proximal weakness, pseudohypertrophy of calf muscles, mild facial weakness, and borderline intelligence. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3422901001000118 Gliedergürtelmuskeldystrophie durch POMK-Mangel de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3422901001000118 Gliedergürtelmuskeldystrophie durch POMK-Mangel 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
Limb girdle muscular dystrophy due to POMK deficiency Is a Inherited metabolic disorder of nervous system true Inferred relationship Existential restriction modifier (core metadata concept)
Limb girdle muscular dystrophy due to POMK deficiency Is a Chronic nervous system disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Limb girdle muscular dystrophy due to POMK deficiency Is a Chronic metabolic disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Limb girdle muscular dystrophy due to POMK deficiency Is a Carbohydrate-deficient glycoprotein syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Limb girdle muscular dystrophy due to POMK deficiency Is a Autosomal recessive muscular dystrophy with limb girdle distribution (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Limb girdle muscular dystrophy due to POMK deficiency Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3
Limb girdle muscular dystrophy due to POMK deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Limb girdle muscular dystrophy due to POMK deficiency Finding site Nervous system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Limb girdle muscular dystrophy due to POMK deficiency Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Limb girdle muscular dystrophy due to POMK deficiency Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Limb girdle muscular dystrophy due to POMK deficiency Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Limb girdle muscular dystrophy due to POMK deficiency Is a Developmental delay true Inferred relationship Existential restriction modifier (core metadata concept)
Limb girdle muscular dystrophy due to POMK deficiency Occurrence Infancy true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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