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1172703004: Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4635469019 POGLUT1-related limb girdle muscular dystrophy R21 en Synonym Active Entire term case sensitive SNOMED CT core module
4635470018 Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
4635471019 Limb girdle muscular dystrophy type 2Z en Synonym Active Only initial character case insensitive SNOMED CT core module
4635472014 Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 en Synonym Active Only initial character case insensitive SNOMED CT core module
4635473016 Autosomal recessive limb girdle muscular dystrophy type 2Z 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
Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 Is a Chronic metabolic disorder true Inferred relationship Existential restriction modifier
Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 Is a Carbohydrate-deficient glycoprotein syndrome true Inferred relationship Existential restriction modifier
Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Existential restriction modifier
Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 Occurrence Adulthood true Inferred relationship Existential restriction modifier 1
Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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