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 |
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