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719985001: Autosomal dominant limb girdle muscular dystrophy type 1A (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3318715013 Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3318716014 Autosomal dominant limb girdle muscular dystrophy type 1A en Synonym Active Only initial character case insensitive SNOMED CT core module
3318717017 Limb girdle muscular dystrophy due to myotilin deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3318719019 Limb-girdle muscular dystrophy 1A myotilin myopathy en Synonym Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant limb girdle muscular dystrophy type 1A Is a Autosomal dominant muscular dystrophy with limb girdle distribution true Inferred relationship Existential restriction modifier
Autosomal dominant limb girdle muscular dystrophy type 1A Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1A Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 3
Autosomal dominant limb girdle muscular dystrophy type 1A Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1A Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal dominant limb girdle muscular dystrophy type 1A Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 3
Autosomal dominant limb girdle muscular dystrophy type 1A Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb girdle muscular dystrophy type 1A Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb girdle muscular dystrophy type 1A Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal dominant limb girdle muscular dystrophy type 1A Clinical course Progressive true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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