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367601000119103: Hereditary amyloidosis (disorder)


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
4022351000052119 ärftlig amyloidos sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


28 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

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
kornealdystrofi, lattice, typ 2 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
familjär amyloid polyneuropati typ 5 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
ärftlig cystatin C-amyloid angiopati 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

Reference Sets

GB English

US English

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