49793008: Hereditary motor neuron disease (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary motor neuron disease

\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary motor neuron disease
\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary motor neuron disease
\Disorder of body system\Disease of nervous system (disorder)\Motor neuron disease\Hereditary motor neuron disease

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

82938010 Familial motor neuron disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

82941018 Hereditary motor neuron disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

787510011 Hereditary motor neuron disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

82938010 Familial motor neuron disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

82938010 Familial motor neuron disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

82941018 Hereditary motor neuron disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

82941018 Hereditary motor neuron disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

787510011 Hereditary motor neuron disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

787510011 Hereditary motor neuron disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

6309971000241119 maladie héréditaire des neurones moteurs fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6309981000241117 maladie héréditaire des motoneurones fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6309971000241119 maladie héréditaire des neurones moteurs fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6309981000241117 maladie héréditaire des motoneurones fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary motor neuron disease	Is a	Hereditary disorder of nervous system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary motor neuron disease	Is a	Familial disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary motor neuron disease	Is a	Motor neuron disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary motor neuron disease	Associated morphology	dégénérescence	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary motor neuron disease	Finding site	Motor neuron (cell)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary motor neuron disease	Finding site	Nervous system structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Spinal muscular atrophy	Is a	True	Hereditary motor neuron disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Juvenile primary lateral sclerosis (disorder)	Is a	True	Hereditary motor neuron disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Neurogenic scapuloperoneal syndrome Kaeser type (disorder)	Is a	True	Hereditary motor neuron disease	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets