FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

715340002: Autosomal recessive limb girdle muscular dystrophy type 2D (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302268016 Alpha-sarcoglycanopathy LGMD2D (limb girdle muscular dystrophy type 2D) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302279014 Autosomal recessive limb girdle muscular dystrophy type 2D (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302280012 Autosomal recessive limb girdle muscular dystrophy type 2D en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302281011 Limb girdle muscular dystrophy characterized by limb-girdle weakness and calf pseudohypertrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3302282016 Limb girdle muscular dystrophy characterised by limb-girdle weakness and calf pseudohypertrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive limb girdle muscular dystrophy type 2D (disorder) Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal recessive limb girdle muscular dystrophy type 2D (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2D (disorder) Finding site Skeletal muscle structure true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2D (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2D (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start