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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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypomyelinating neuropathy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital hypomyelinating neuropathy morphologie associée (attribut) structure anormale sur le plan morphologique false Inferred relationship Some 1
Congenital hypomyelinating neuropathy survenue (attribut) congénital true Inferred relationship Some 1
Congenital hypomyelinating neuropathy localisation d'une constatation (attribut) structure d'un nerf true Inferred relationship Some 1
Congenital hypomyelinating neuropathy morphologie associée (attribut) Hypomyelination true Inferred relationship Some 1
Congenital hypomyelinating neuropathy est un(e) (attribut) Congenital anomaly of nervous system true Inferred relationship Some
Congenital hypomyelinating neuropathy est un(e) (attribut) anomalie congénitale du système nerveux périphérique false Inferred relationship Some
Congenital hypomyelinating neuropathy est un(e) (attribut) Neuropathy (disorder) true Inferred relationship Some
Congenital hypomyelinating neuropathy morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Congenital hypomyelinating neuropathy morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Congenital hypomyelinating neuropathy localisation d'une constatation (attribut) structure du système nerveux périphérique false Inferred relationship Some 1
Congenital hypomyelinating neuropathy est un(e) (attribut) Congenital polyneuropathy false Inferred relationship Some
Congenital hypomyelinating neuropathy survenue (attribut) congénital false Inferred relationship Some
Congenital hypomyelinating neuropathy localisation d'une constatation (attribut) structure du système nerveux périphérique false Inferred relationship Some 1
Congenital hypomyelinating neuropathy localisation d'une constatation (attribut) structure d'un nerf false Inferred relationship Some 2
Congenital hypomyelinating neuropathy survenue (attribut) congénital false Inferred relationship Some 2
Congenital hypomyelinating neuropathy morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
Congenital hypomyelinating neuropathy localisation d'une constatation (attribut) structure du système nerveux périphérique false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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