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

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
359677016 Autosomal dominant muscular dystrophy not predominantly limb girdle en Synonym Active Entire term case insensitive SNOMED CT core module
629168016 Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core 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 Is a Muscular dystrophy not predominantly limb girdle in distribution true Inferred relationship Existential restriction modifier
Autosomal dominant muscular dystrophy not predominantly limb girdle Is a Congenital hereditary muscular dystrophy true Inferred relationship Existential restriction modifier
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant muscular dystrophy not predominantly limb girdle Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Occurrence Congenital false Inferred relationship Existential restriction modifier
Autosomal dominant muscular dystrophy not predominantly limb girdle Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Autosomal dominant muscular dystrophy not predominantly limb girdle Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Autosomal dominant muscular dystrophy not predominantly limb girdle Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 3
Autosomal dominant muscular dystrophy not predominantly limb girdle Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant muscular dystrophy not predominantly limb girdle Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal dominant muscular dystrophy not predominantly limb girdle Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal dominant muscular dystrophy not predominantly limb girdle Clinical course Progressive true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Benign scapuloperoneal muscular dystrophy Is a True Autosomal dominant muscular dystrophy not predominantly limb girdle Inferred relationship Existential restriction modifier
Severe scapuloperoneal muscular dystrophy with cardiomyopathy Is a False Autosomal dominant muscular dystrophy not predominantly limb girdle Inferred relationship Existential restriction modifier
Benign congenital muscular dystrophy with finger flexion contractures Is a True Autosomal dominant muscular dystrophy not predominantly limb girdle Inferred relationship Existential restriction modifier
Distal muscular dystrophy with adult onset Is a False Autosomal dominant muscular dystrophy not predominantly limb girdle Inferred relationship Existential restriction modifier
Facioscapulohumeral muscular dystrophy Is a False Autosomal dominant muscular dystrophy not predominantly limb girdle Inferred relationship Existential restriction modifier
Oculopharyngeal muscular dystrophy Is a True Autosomal dominant muscular dystrophy not predominantly limb girdle Inferred relationship Existential restriction modifier
Facioscapulohumeral muscular dystrophy Is a True Autosomal dominant muscular dystrophy not predominantly limb girdle Inferred relationship Existential restriction modifier
Distal myopathy 2 Is a False Autosomal dominant muscular dystrophy not predominantly limb girdle Inferred relationship Existential restriction modifier
Distal myopathy Welander type Is a False Autosomal dominant muscular dystrophy not predominantly limb girdle Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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