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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

30 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
Lattice corneal dystrophy Type II Is a False Hereditary amyloidosis (disorder) Inferred relationship Some
Transthyretin related familial amyloid cardiomyopathy (disorder) Is a False 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
Hereditary transthyretin related amyloidosis (disorder) Is a True Hereditary amyloidosis (disorder) Inferred relationship Some

This concept is not in any reference sets

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