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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 Reference Sets
345474019 Congenital hypomyelinating neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
345475018 Lyon's hypomyelinating neuropathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
618389011 Congenital hypomyelinating neuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
2105491000052119 kongenital hypomyeliniseringsneuropati sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept) Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypomyelinating neuropathy Is a Congenital polyneuropathy false Inferred relationship Some
Congenital hypomyelinating neuropathy Occurrence Congenital false Inferred relationship Some
Congenital hypomyelinating neuropathy Finding site Peripheral nervous system structure false Inferred relationship Some 1
Congenital hypomyelinating neuropathy Finding site Nerve structure false Inferred relationship Some 2
Congenital hypomyelinating neuropathy Is a Congenital anomaly of the peripheral nervous system false Inferred relationship Some
Congenital hypomyelinating neuropathy Is a Neuropathy (disorder) true Inferred relationship Some
Congenital hypomyelinating neuropathy Associated morphology kongenital anomali false Inferred relationship Some 1
Congenital hypomyelinating neuropathy Associated morphology kongenital anomali false Inferred relationship Some 1
Congenital hypomyelinating neuropathy Finding site Peripheral nervous system structure false Inferred relationship Some 1
Congenital hypomyelinating neuropathy Occurrence Congenital false Inferred relationship Some 2
Congenital hypomyelinating neuropathy Associated morphology Developmental anomaly (morphologic abnormality) false Inferred relationship Some 2
Congenital hypomyelinating neuropathy Finding site Peripheral nervous system structure false Inferred relationship Some 2
Congenital hypomyelinating neuropathy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital hypomyelinating neuropathy Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 1
Congenital hypomyelinating neuropathy Occurrence Congenital true Inferred relationship Some 1
Congenital hypomyelinating neuropathy Finding site Nerve structure true Inferred relationship Some 1
Congenital hypomyelinating neuropathy Associated morphology Hypomyelination true Inferred relationship Some 1
Congenital hypomyelinating neuropathy Is a Congenital anomaly of nervous system true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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