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367601000119103: hereditaire amyloïdose (aandoening)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3482130011 Hereditary amyloidosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3482131010 Hereditary amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6188681000146113 hereditaire amyloïdose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6188691000146110 hereditaire amyloïdose (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6826311000146114 erfelijke amyloïdose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


29 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary amyloidosis (disorder) Associated morphology Amyloid deposition true Inferred relationship Some 1
Hereditary amyloidosis (disorder) Is a Amyloidosis true Inferred relationship Some
Hereditary amyloidosis (disorder) Is a Hereditary disease true Inferred relationship Some
Hereditary amyloidosis (disorder) Is a Hereditary metabolic disease false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial Mediterranean fever Is a False Hereditary amyloidosis (disorder) Inferred relationship Some
Familial amyloid nephropathy with urticaria AND deafness Is a True Hereditary amyloidosis (disorder) Inferred relationship Some
Hereditary oculoleptomeningeal amyloid angiopathy Is a True Hereditary amyloidosis (disorder) Inferred relationship Some
Familial amyloid polyneuropathy with cutaneous amyloidosis (disorder) Is a False Hereditary amyloidosis (disorder) Inferred relationship Some
'lattice'-corneadystrofie type 2 (aandoening) Is a False Hereditary amyloidosis (disorder) Inferred relationship Some
Transthyretin related familial amyloid cardiomyopathy (disorder) Is a True Hereditary amyloidosis (disorder) Inferred relationship Some
Autosomal dominant beta2-microglobulinic amyloidosis (disorder) Is a True Hereditary amyloidosis (disorder) Inferred relationship Some
Hereditary cerebral hemorrhage with amyloidosis (disorder) Is a False Hereditary amyloidosis (disorder) Inferred relationship Some
Prion protein systemic amyloidosis (disorder) Is a True Hereditary amyloidosis (disorder) Inferred relationship Some
Familial dementia British type (disorder) Is a False Hereditary amyloidosis (disorder) Inferred relationship Some
AGel amyloidosis Is a True Hereditary amyloidosis (disorder) Inferred relationship Some
ADan amyloidosis Is a False Hereditary amyloidosis (disorder) Inferred relationship Some
Meretoja syndrome Is a False Hereditary amyloidosis (disorder) Inferred relationship Some
Heredofamilial systemic amyloidosis affecting skin (disorder) Is a True Hereditary amyloidosis (disorder) Inferred relationship Some
Familial amyloid polyneuropathy (disorder) Is a True Hereditary amyloidosis (disorder) Inferred relationship Some
Gelatinous droplike corneal dystrophy (disorder) Is a True Hereditary amyloidosis (disorder) Inferred relationship Some
Hereditary cystatin C amyloid angiopathy Is a False Hereditary amyloidosis (disorder) Inferred relationship Some
Lattice corneal dystrophy (disorder) Is a False Hereditary amyloidosis (disorder) Inferred relationship Some
Localised hereditary amyloidosis Is a True Hereditary amyloidosis (disorder) Inferred relationship Some
Hereditary cerebrovascular amyloidosis Is a True Hereditary amyloidosis (disorder) Inferred relationship Some
Integral membrane protein 2B related amyloidosis (disorder) Is a True Hereditary amyloidosis (disorder) Inferred relationship Some

This concept is not in any reference sets

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