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37959007: Transthyretin (substance)


Status: current, Not 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
63317014 Prealbumin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
63318016 Transthyretin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5197713014 Thyroxine binding prealbumin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5197714015 TBPA - thyroxine binding prealbumin en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5197715019 Transthyretin (substance) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
178041000077116 préalbumine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Prealbumin Is a Albumin false Inferred relationship Some
Prealbumin Is a Protein true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Transthyretin measurement Has measured component (attribute) False Prealbumin Inferred relationship Some
Prealbumin measurement Has measured component (attribute) False Prealbumin Inferred relationship Some
Transthyretin measurement Component True Prealbumin Inferred relationship Some 1
Prealbumin measurement Component False Prealbumin Inferred relationship Some
Serum prealbumin level (procedure) Component False Prealbumin Inferred relationship Some 2
Senile cardiac amyloidosis Causative agent (attribute) True Prealbumin Inferred relationship Some 1
A rare hereditary Transthyretin (TTR)-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein. Causative agent (attribute) True Prealbumin Inferred relationship Some 1
Wild type ATTR amyloidosis (disorder) Causative agent (attribute) True Prealbumin Inferred relationship Some 1
Hereditary oculoleptomeningeal amyloid angiopathy Causative agent (attribute) True Prealbumin Inferred relationship Some 1
Serum prealbumin level (procedure) Component True Prealbumin Inferred relationship Some 1
A rare genetic systemic disease characterized by adult onset, progressive sensorimotor and autonomic neuropathy and infiltrative cardiomyopathy. Neurological involvement usually starts with sensory loss in the extremities and progresses with motor neuropathy. Cardiomyopathy presents with rhythm abnormalities and heart failure. The disease also frequently manifests with a range of additional clinical signs and symptoms due to associated ocular, renal, central nervous system and gastrointestinal involvement. Causative agent (attribute) True Prealbumin Inferred relationship Some 1

This concept is not in any reference sets

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