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42295001: Familial amyloid polyneuropathy (disorder)


Status: current, 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
100421000077110 neuropathie amyloïde familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3035568014 Neuropathic heredofamilial amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
371661000077110 neuropathie amyloïde familiale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
493270014 Familial neuropathic amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
70562011 Familial amyloid polyneuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
70564012 AF type amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
70566014 Familial polyneuropathic amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
779178017 Familial amyloid polyneuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
neuropathie amyloïde familiale est un(e) (attribut) Hereditary amyloidosis (disorder) true Inferred relationship Some
neuropathie amyloïde familiale est un(e) (attribut) Systemic amyloidosis true Inferred relationship Some
neuropathie amyloïde familiale localisation d'une constatation (attribut) nerf périphérique (structure corporelle) true Inferred relationship Some 1
neuropathie amyloïde familiale est un(e) (attribut) Hereditary peripheral neuropathy true Inferred relationship Some
neuropathie amyloïde familiale est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
neuropathie amyloïde familiale est un(e) (attribut) polyneuropathie true Inferred relationship Some
neuropathie amyloïde familiale est un(e) (attribut) Familial disease true Inferred relationship Some
neuropathie amyloïde familiale est un(e) (attribut) amyloïdose localisée false Inferred relationship Some
neuropathie amyloïde familiale est un(e) (attribut) Amyloidosis false Inferred relationship Some
neuropathie amyloïde familiale est un(e) (attribut) lésion neurologique false Inferred relationship Some
neuropathie amyloïde familiale morphologie associée (attribut) Amyloid deposition true Inferred relationship Some 1
neuropathie amyloïde familiale localisation d'une constatation (attribut) structure du système nerveux périphérique false Inferred relationship Some 1
neuropathie amyloïde familiale localisation d'une constatation (attribut) nerf périphérique (structure corporelle) false Inferred relationship Some 2
neuropathie amyloïde familiale est un(e) (attribut) affection dégénérative false Inferred relationship Some
neuropathie amyloïde familiale localisation d'une constatation (attribut) structure du système nerveux périphérique false Inferred relationship Some 1
neuropathie amyloïde familiale morphologie associée (attribut) Amyloid deposition false Inferred relationship Some 1
neuropathie amyloïde familiale localisation d'une constatation (attribut) structure d'un nerf false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial amyloid neuropathy, Finnish type est un(e) (attribut) False neuropathie amyloïde familiale Inferred relationship Some
Glomerular disorder due to neuropathic heredofamilial amyloidosis Due to True neuropathie amyloïde familiale Inferred relationship Some 2
Amyloidosis, type I est un(e) (attribut) False neuropathie amyloïde familiale Inferred relationship Some
Familial amyloid polyneuropathy, Jewish type est un(e) (attribut) False neuropathie amyloïde familiale Inferred relationship Some
Familial amyloid polyneuropathy, type II est un(e) (attribut) True neuropathie amyloïde familiale Inferred relationship Some
Amyloid polyneuropathy type I (disorder) est un(e) (attribut) True neuropathie amyloïde familiale Inferred relationship Some
Familial amyloid polyneuropathy with cutaneous amyloidosis (disorder) est un(e) (attribut) True neuropathie amyloïde familiale Inferred relationship Some
Familial amyloid polyneuropathy, type VI (disorder) est un(e) (attribut) True neuropathie amyloïde familiale Inferred relationship Some
Familial amyloid polyneuropathy, Jewish type est un(e) (attribut) True neuropathie amyloïde familiale Inferred relationship Some
Familial amyloid polyneuropathy, Iowa type est un(e) (attribut) True neuropathie amyloïde familiale Inferred relationship Some
Amyloid polyneuropathy type I est un(e) (attribut) False neuropathie amyloïde familiale Inferred relationship Some

Reference Sets

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

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