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1230273004: Megaconial congenital muscular dystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5068648018 Congenital muscular dystrophy with mitochondrial structural abnormalities en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5068649014 Megaconial congenital muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5068650014 Megaconial congenital muscular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5068651013 Congenital megaconial myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5068652018 Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5068653011 A rare genetic, skeletal muscle disease with characteristics of early-onset hypotonia, muscle weakness, global developmental delay with intellectual disability and cardiomyopathy. Congenital structural heart defects and ichthyosiform cutaneous lesions have also been associated. Muscle biopsy shows characteristic enlarged mitochondria located at the periphery of muscle fibres. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5068654017 A rare genetic, skeletal muscle disease with characteristics of early-onset hypotonia, muscle weakness, global developmental delay with intellectual disability and cardiomyopathy. Congenital structural heart defects and ichthyosiform cutaneous lesions have also been associated. Muscle biopsy shows characteristic enlarged mitochondria located at the periphery of muscle fibers. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5068648018 Congenital muscular dystrophy with mitochondrial structural abnormalities en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5068649014 Megaconial congenital muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5068650014 Megaconial congenital muscular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5068651013 Congenital megaconial myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5068652018 Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5068653011 A rare genetic, skeletal muscle disease with characteristics of early-onset hypotonia, muscle weakness, global developmental delay with intellectual disability and cardiomyopathy. Congenital structural heart defects and ichthyosiform cutaneous lesions have also been associated. Muscle biopsy shows characteristic enlarged mitochondria located at the periphery of muscle fibres. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5068654017 A rare genetic, skeletal muscle disease with characteristics of early-onset hypotonia, muscle weakness, global developmental delay with intellectual disability and cardiomyopathy. Congenital structural heart defects and ichthyosiform cutaneous lesions have also been associated. Muscle biopsy shows characteristic enlarged mitochondria located at the periphery of muscle fibers. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
651951000274112 Megakoniale kongenitale Muskeldystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
651951000274112 Megakoniale kongenitale Muskeldystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3391201001000115 Langketten-3-Hydroxyacyl-CoA-Dehydrogenase-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
Megaconial congenital muscular dystrophy (disorder) Is a Congenital hereditary muscular dystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Megaconial congenital muscular dystrophy (disorder) Is a Inherited metabolic disorder of nervous system true Inferred relationship Existential restriction modifier (core metadata concept)
Megaconial congenital muscular dystrophy (disorder) Is a Chronic nervous system disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Megaconial congenital muscular dystrophy (disorder) Is a Chronic metabolic disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Megaconial congenital muscular dystrophy (disorder) Is a Disorder of lipid metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Megaconial congenital muscular dystrophy (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Megaconial congenital muscular dystrophy (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 4
Megaconial congenital muscular dystrophy (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Megaconial congenital muscular dystrophy (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Megaconial congenital muscular dystrophy (disorder) Associated morphology Mitochondrial enlargement true Inferred relationship Existential restriction modifier (core metadata concept) 1
Megaconial congenital muscular dystrophy (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Megaconial congenital muscular dystrophy (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Megaconial congenital muscular dystrophy (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Megaconial congenital muscular dystrophy (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Megaconial congenital muscular dystrophy (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Megaconial congenital muscular dystrophy (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Megaconial congenital muscular dystrophy (disorder) Finding site Nervous system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Megaconial congenital muscular dystrophy (disorder) Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
Megaconial congenital muscular dystrophy (disorder) Is a Chronic mental disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Megaconial congenital muscular dystrophy (disorder) Is a Global developmental delay true Inferred relationship Existential restriction modifier (core metadata concept)
Megaconial congenital muscular dystrophy (disorder) Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 5
Megaconial congenital muscular dystrophy (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Megaconial congenital muscular dystrophy (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 6
Megaconial congenital muscular dystrophy (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 6

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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