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89010004: Rhabdomyolysis (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
147583011 Rhabdomyolysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
831814018 Rhabdomyolysis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
50007051000188111 rhabdomyolyse 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
Rhabdomyolysis Is a Lysis false Inferred relationship Some
Rhabdomyolysis Is a Lysis (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Equine rhabdomyolysis Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Exertional rhabdomyolysis Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Traumatic rhabdomyolysis Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Rhabdomyolysis Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Non-traumatic rhabdomyolysis (disorder) Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Familial paroxysmal rhabdomyolysis Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Myoglobinuria following ingestion of eel Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Haff syndrome Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Porcine stress syndrome Associated morphology False Rhabdomyolysis Inferred relationship Some 1
March myoglobinuria Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Equine polysaccharide storage myopathy Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Exertional rhabdomyolysis Associated morphology True Rhabdomyolysis Inferred relationship Some 1
Myoglobinuria following ingestion of eel Associated morphology True Rhabdomyolysis Inferred relationship Some 1
Haff syndrome Associated morphology True Rhabdomyolysis Inferred relationship Some 1
Equine rhabdomyolysis Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Porcine stress syndrome Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Equine polysaccharide storage myopathy Associated morphology False Rhabdomyolysis Inferred relationship Some 1
Non-traumatic rhabdomyolysis (disorder) Associated morphology True Rhabdomyolysis Inferred relationship Some 1
Familial paroxysmal rhabdomyolysis Associated morphology True Rhabdomyolysis Inferred relationship Some 1
Traumatic rhabdomyolysis Associated morphology True Rhabdomyolysis Inferred relationship Some 1
Rhabdomyolysis Associated morphology True Rhabdomyolysis Inferred relationship Some 1
March myoglobinuria Associated morphology True Rhabdomyolysis Inferred relationship Some 1
Secondary rhabdomyolysis (disorder) Associated morphology True Rhabdomyolysis Inferred relationship Some 2
Rhabdomyolysis due to statin (disorder) Associated morphology True Rhabdomyolysis Inferred relationship Some 1
Rhabdomyolysis due to disease caused by severe acute respiratory syndrome coronavirus 2 (disorder) Associated morphology True Rhabdomyolysis Inferred relationship Some 2
Crush syndrome Associated morphology True Rhabdomyolysis Inferred relationship Some 1
Paroxysmal rhabdomyolysis (disorder) Associated morphology True Rhabdomyolysis Inferred relationship Some 1
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome is a rare, genetic, neurodegenerative disease characterized by episodic metabolic encephalomyopathic crises (of variable frequency and severity which are frequently precipitated by an acute illness) which manifest with profound muscle weakness, ataxia, seizures, cardiac arrhythmias, rhabdomyolysis with myoglobinuria, elevated plasma creatine kinase, hypoglycemia, lactic acidosis, increased acylcarnitines and a disorientated or comatose state. Global developmental delay, intellectual disability and cortical, pyramidal and cerebellar signs develop with subsequent progressive neurodegeneration causing loss of expressive language and varying degrees of cerebral atrophy. Associated morphology True Rhabdomyolysis Inferred relationship Some 3

This concept is not in any reference sets

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