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240075007: Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder)


Status: current, 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
359677016 Autosomal dominant muscular dystrophy not predominantly limb girdle en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
629168016 Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
359677016 Autosomal dominant muscular dystrophy not predominantly limb girdle en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
359677016 Autosomal dominant muscular dystrophy not predominantly limb girdle en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
629168016 Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
629168016 Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5036551000241118 dystrophie musculaire autosomique dominante pas prédominante à la ceinture fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5036551000241118 dystrophie musculaire autosomique dominante pas prédominante à la ceinture fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Is a Muscular dystrophy not predominantly limb girdle in distribution true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Is a Congenital hereditary muscular dystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Benign scapuloperoneal muscular dystrophy Is a True Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Severe scapuloperoneal muscular dystrophy with cardiomyopathy Is a False Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Benign congenital muscular dystrophy with finger flexion contractures Is a True Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Distal muscular dystrophy with adult onset Is a False Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Facioscapulohumeral muscular dystrophy Is a False Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Oculopharyngeal muscular dystrophy Is a True Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Facioscapulohumeral muscular dystrophy (disorder) Is a True Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Distal myopathy 2 Is a False Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Distal myopathy Welander type (disorder) Is a False Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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