128206006: Congenital sensory neuropathy with selective loss of small myelinated fibers (disorder)

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

\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\...

\Inherited autonomic nervous system disorder (disorder)\Hereditary sensory and autonomic neuropathy\Congenital sensory neuropathy with selective loss of small myelinated fibres

\Hereditary peripheral neuropathy\Hereditary sensory and autonomic neuropathy\Congenital sensory neuropathy with selective loss of small myelinated fibres

\Disorder of foetus and/or newborn\Congenital disease\Congenital sensory neuropathy with selective loss of small myelinated fibres

\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Inherited autonomic nervous system disorder (disorder)\Hereditary sensory and autonomic neuropathy\Congenital sensory neuropathy with selective loss of small myelinated fibres
\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary peripheral neuropathy\Hereditary sensory and autonomic neuropathy\Congenital sensory neuropathy with selective loss of small myelinated fibres
\Disorder of body system\Disease of nervous system (disorder)\Neuropathy\Hereditary sensory and autonomic neuropathy\Congenital sensory neuropathy with selective loss of small myelinated fibres
\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Inherited autonomic nervous system disorder (disorder)\Hereditary sensory and autonomic neuropathy\Congenital sensory neuropathy with selective loss of small myelinated fibres
\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Hereditary peripheral neuropathy\Hereditary sensory and autonomic neuropathy\Congenital sensory neuropathy with selective loss of small myelinated fibres
\Disorder of body system\Disease of nervous system (disorder)\Disorder of the peripheral nervous system (disorder)\Hereditary peripheral neuropathy\Hereditary sensory and autonomic neuropathy\Congenital sensory neuropathy with selective loss of small myelinated fibres
\Disorder of body system\Disease of nervous system (disorder)\Disorder of autonomic nervous system\Inherited autonomic nervous system disorder (disorder)\Hereditary sensory and autonomic neuropathy\Congenital sensory neuropathy with selective loss of small myelinated fibres

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital sensory neuropathy with selective loss of small myelinated fibres	Is a	Hereditary sensory and autonomic neuropathy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital sensory neuropathy with selective loss of small myelinated fibres	Finding site	Autonomic nerve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital sensory neuropathy with selective loss of small myelinated fibres	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital sensory neuropathy with selective loss of small myelinated fibres	Finding site	Autonomic nervous system structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital sensory neuropathy with selective loss of small myelinated fibres	Finding site	Nerve structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital sensory neuropathy with selective loss of small myelinated fibres	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital sensory neuropathy with selective loss of small myelinated fibres	Finding site	Peripheral nervous system structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital sensory neuropathy with selective loss of small myelinated fibres	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital sensory neuropathy with selective loss of small myelinated fibres	Finding site	Nerve structure	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

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
206446018	Hereditary sensory and autonomic neuropathy, type V	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
206447010	HSAN V	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
206448017	Congenital sensory neuropathy with selective loss of small myelinated fibres	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
474344010	Hereditary sensory and autonomic neuropathy type V	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474345011	Congenital sensory neuropathy with selective loss of small myelinated fibers	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
732171018	Congenital sensory neuropathy with selective loss of small myelinated fibers (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
206446018	Hereditary sensory and autonomic neuropathy, type V	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
206447010	HSAN V	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
206448017	Congenital sensory neuropathy with selective loss of small myelinated fibres	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
206448017	Congenital sensory neuropathy with selective loss of small myelinated fibres	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
474344010	Hereditary sensory and autonomic neuropathy type V	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474345011	Congenital sensory neuropathy with selective loss of small myelinated fibers	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474345011	Congenital sensory neuropathy with selective loss of small myelinated fibers	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
732171018	Congenital sensory neuropathy with selective loss of small myelinated fibers (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
732171018	Congenital sensory neuropathy with selective loss of small myelinated fibers (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3427901001000115	Neuropathie, autonome hereditäre sensorische, Typ 5	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
126641000077114	neuropathie sensitive congénitale avec perte sélective des petites fibres myélinisées	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
126641000077114	neuropathie sensitive congénitale avec perte sélective des petites fibres myélinisées	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3427901001000115	Neuropathie, autonome hereditäre sensorische, Typ 5	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module