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698836007: Spinal cord myoclonus (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2981357014 Spinal cord myoclonus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2981369018 Spinal cord myoclonus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2981383016 Spinal myoclonus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6015441000241119 myoclonie provenant de la moelle spinale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6015451000241116 myoclonie spinale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6015461000241118 myoclonie provenant de la moelle épinière fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spinal cord myoclonus Is a Spinal cord disorder (disorder) true Inferred relationship Some
Spinal cord myoclonus Is a Myoclonic disorder true Inferred relationship Some
Spinal cord myoclonus Finding site Spinal cord structure true Inferred relationship Some 1
Spinal cord myoclonus Interprets mouvement false Inferred relationship Some 2
Spinal cord myoclonus Interprets Movement observable true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Paramyoclonus multiplex Is a True Spinal cord myoclonus Inferred relationship Some
Segmental cord myoclonus Is a True Spinal cord myoclonus Inferred relationship Some
Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome is a rare hereditary spastic ataxia disorder characterized by childhood onset of slowly progressive lower limb spastic paraparesis and cerebellar ataxia (with dysarthria, swallowing difficulties, motor degeneration), associated with sensorimotor neuropathy (including muscle weakness and distal amyotrophy in lower extremities) and progressive myoclonic epilepsy. Ocular signs (ptosis, oculomotor apraxia), dysmetria, dysdiadochokinesia, dystonic movements and myoclonus may also be associated. Is a False Spinal cord myoclonus Inferred relationship Some

This concept is not in any reference sets

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