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5523002: Idiopathic myoglobinuria (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
10212016 Idiopathic myoglobinuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
10213014 Spontaneous myoglobinuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
10214015 Meyer-Betz disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
10215019 Acute paroxysmal myoglobinuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
793550012 Idiopathic myoglobinuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1231436012 Non-exertional myoglobinuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
10212016 Idiopathic myoglobinuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
10212016 Idiopathic myoglobinuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
10213014 Spontaneous myoglobinuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
10213014 Spontaneous myoglobinuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
10214015 Meyer-Betz disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
10215019 Acute paroxysmal myoglobinuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
10215019 Acute paroxysmal myoglobinuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
793550012 Idiopathic myoglobinuria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
793550012 Idiopathic myoglobinuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1231436012 Non-exertional myoglobinuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1231436012 Non-exertional myoglobinuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1231437015 Paroxysmal rhabdomyolysis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1231437015 Paroxysmal rhabdomyolysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
291311000077118 myoglobinurie idiopathique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
291311000077118 myoglobinurie idiopathique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Idiopathic myoglobinuria Is a Acute disease of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic myoglobinuria Is a Disorder of skeletal muscle false Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic myoglobinuria Finding site Muscle tissue false Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic myoglobinuria Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Idiopathic myoglobinuria Course Acute false Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic myoglobinuria Onset Acute onset false Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic myoglobinuria Course Acute false Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic myoglobinuria Clinical course Sudden onset AND/OR short duration (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Idiopathic myoglobinuria Is a Idiopathic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic myoglobinuria Interprets Myoglobin measurement, urine true Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic myoglobinuria Has interpretation Present (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic myoglobinuria Interprets Urine observable false Inferred relationship Existential restriction modifier (core metadata concept) 2
Idiopathic myoglobinuria Is a Myoglobinuria true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic myoglobinuria Is a Acute disease true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic myoglobinuria Is a Abnormal urinary product true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic myoglobinuria Has interpretation Detected (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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