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715655000: Transthyretin related familial amyloid cardiomyopathy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3303311010 Transthyretin related familial amyloid cardiomyopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3303312015 Transthyretin related familial amyloid cardiomyopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3303313013 Transthyretin amyloid cardiopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3303314019 ATTRV122I amyloidosis en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Transthyretin related familial amyloid cardiomyopathy Associated morphology Amyloid deposition true Inferred relationship Existential restriction modifier 1
Transthyretin related familial amyloid cardiomyopathy Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Transthyretin related familial amyloid cardiomyopathy Is a Familial restrictive cardiomyopathy true Inferred relationship Existential restriction modifier
Transthyretin related familial amyloid cardiomyopathy Is a Familial non-neuropathic amyloidosis false Inferred relationship Existential restriction modifier
Transthyretin related familial amyloid cardiomyopathy Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Transthyretin related familial amyloid cardiomyopathy Finding site Myocardium structure false Inferred relationship Existential restriction modifier 2
Transthyretin related familial amyloid cardiomyopathy Is a Hereditary amyloidosis true Inferred relationship Existential restriction modifier
Transthyretin related familial amyloid cardiomyopathy Is a Myocardial degeneration false Inferred relationship Existential restriction modifier
Transthyretin related familial amyloid cardiomyopathy Finding site Myocardium structure true Inferred relationship Existential restriction modifier 1
Transthyretin related familial amyloid cardiomyopathy Causative agent Prealbumin true Inferred relationship Existential restriction modifier 1
Transthyretin related familial amyloid cardiomyopathy Is a Infiltrative cardiomyopathy true Inferred relationship Existential restriction modifier
Transthyretin related familial amyloid cardiomyopathy Is a Familial non-neuropathic amyloidosis of heart true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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