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37340000: Motor neuron disease (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
62293019 Motor neuron disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
486695013 Motor neurone disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769196010 Motor neuron disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5372519013 MND - motor neuron disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5372732017 MND - motor neurone disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1833291000195118 malattia del motoneurone it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
553751000172114 maladie du motoneurone fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
602551000172110 maladie du neurone moteur fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

91 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Motor neuron disease Is a Disorder of nervous system (disorder) true Inferred relationship Some
Motor neuron disease Is a Degenerative disorder false Inferred relationship Some
Motor neuron disease Associated morphology dégénérescence false Inferred relationship Some 2
Motor neuron disease Finding site Motor neuron false Inferred relationship Some
Motor neuron disease Finding site Structure of nervous system (body structure) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Western Pacific motor neurone disease Is a True Motor neuron disease Inferred relationship Some
Madras-type motor neurone disease Is a True Motor neuron disease Inferred relationship Some
Paraneoplastic motor neurone disease Is a True Motor neuron disease Inferred relationship Some
Troyer syndrome Is a True Motor neuron disease Inferred relationship Some
Spastic tetraplegia with rigidity syndrome Is a True Motor neuron disease Inferred relationship Some
Hereditary motor neuron disease Is a True Motor neuron disease Inferred relationship Some
Lower motor neuron disease Is a True Motor neuron disease Inferred relationship Some
Amyotrophic lateral sclerosis Is a True Motor neuron disease Inferred relationship Some
Progressive muscular atrophy Is a True Motor neuron disease Inferred relationship Some
Upper motor neuron disease Is a True Motor neuron disease Inferred relationship Some
Motor neurone disease NOS Is a False Motor neuron disease Inferred relationship Some
Peripheral motor neuropathy Is a False Motor neuron disease Inferred relationship Some
FH: Motor neurone disease Associated finding False Motor neuron disease Inferred relationship Some 1
FH: Motor neurone disease Associated finding True Motor neuron disease Inferred relationship Some 1
FH: Motor neurone disease Associated finding False Motor neuron disease Inferred relationship Some 1
Neuromyotonia Is a True Motor neuron disease Inferred relationship Some
A rare, acquired motor neuron disease characterized by a slowly progressive, unilateral, ascending or descending hemiplegia, associated to unilateral or asymmetrical pyramidal signs and no sensory loss. It is a diagnosis of exclusion and controversy exists regarding whether the presence of bulbar symptoms, sphincter disturbances, fasciculations or cognitive manifestations characterize the disease. Is a True Motor neuron disease Inferred relationship Some
Frontal lobe degeneration with motor neurone disease Is a True Motor neuron disease Inferred relationship Some
Motor neuron disease due to lead intoxication (disorder) Is a True Motor neuron disease Inferred relationship Some
A rare genetic motor neuron disease characterized by decreased or absent fetal movements, congenital proximal and distal joint contractures (consistent with arthrogryposis multiplex congenita), and multiple congenital fractures of the long bones. Further manifestations are neonatal respiratory distress, severe muscular hypotonia, areflexia, dysphagia, congenital heart defects, and dysmorphic facial features. Muscle biopsy shows increased fiber-size variation and grouping of larger type I fibers. The disease is usually fatal in infancy due to respiratory failure. Is a True Motor neuron disease Inferred relationship Some
Motor neuron disease due to gammopathy (disorder) Is a True Motor neuron disease Inferred relationship Some
Motor neuron disease due to herpes zoster (disorder) Is a True Motor neuron disease Inferred relationship Some
Motor neuron disease due to human immunodeficiency virus infection (disorder) Is a True Motor neuron disease Inferred relationship Some
Motor neuron disease due to hereditary spastic paraplegia (disorder) Is a True Motor neuron disease Inferred relationship Some
Motor neuron disease due to and following radiotherapy to spinal cord (disorder) Is a True Motor neuron disease Inferred relationship Some
Motor neuron disease due to neoplastic disease (disorder) Is a True Motor neuron disease Inferred relationship Some
A rare acquired motor neuron disease with characteristics of an initial unilateral weakness in the intrinsic hand muscles that eventually spreads to the opposite limb (with an asymmetrical distribution) and that has a very slow progression of muscular atrophy over a 20 year period. Is a True Motor neuron disease Inferred relationship Some

This concept is not in any reference sets

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