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230562000: Congenital hypomyelinating neuropathy (disorder)

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
345474019 Congenital hypomyelinating neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
345475018 Lyon's hypomyelinating neuropathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
618389011 Congenital hypomyelinating neuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
345474019 Congenital hypomyelinating neuropathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
345474019 Congenital hypomyelinating neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
345475018 Lyon's hypomyelinating neuropathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
618389011 Congenital hypomyelinating neuropathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
618389011 Congenital hypomyelinating neuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4960001000241118 neuropathie congénitale hypomyelinisante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4960001000241118 neuropathie congénitale hypomyelinisante 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
Congenital hypomyelinating neuropathy Is a polyneuropathie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypomyelinating neuropathy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypomyelinating neuropathy Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypomyelinating neuropathy Finding site Nerve structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypomyelinating neuropathy Is a Congenital anomaly of the peripheral nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypomyelinating neuropathy Is a Neuropathy true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypomyelinating neuropathy Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypomyelinating neuropathy Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypomyelinating neuropathy Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypomyelinating neuropathy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypomyelinating neuropathy Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypomyelinating neuropathy Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypomyelinating neuropathy Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypomyelinating neuropathy Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypomyelinating neuropathy Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypomyelinating neuropathy Finding site Nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypomyelinating neuropathy Associated morphology Hypomyelination true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypomyelinating neuropathy Is a Congenital anomaly of nervous system true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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