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56112001: Thyroxine transport defect (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
93320012 Thyroxine transport defect en Synonym Active Entire term case insensitive SNOMED CT core module
794589010 Thyroxine transport defect (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

7 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Thyroxine transport defect Is a Inherited disorder of thyroid metabolism true Inferred relationship Existential restriction modifier
Thyroxine transport defect Interprets Biological transport, function false Inferred relationship Existential restriction modifier
Thyroxine transport defect Finding site Thyroid structure false Inferred relationship Existential restriction modifier
Thyroxine transport defect Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Thyroxine transport defect Occurrence Congenital false Inferred relationship Existential restriction modifier
Thyroxine transport defect Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Thyroxine transport defect Finding site Thyroid structure true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant variant form of albumin Is a True Thyroxine transport defect Inferred relationship Existential restriction modifier
X-linked absence of thyroxine-binding globulin Is a True Thyroxine transport defect Inferred relationship Existential restriction modifier
X-linked reduction of thyroxine-binding globulin Is a True Thyroxine transport defect Inferred relationship Existential restriction modifier
X-linked excess of thyroxine-binding globulin Is a True Thyroxine transport defect Inferred relationship Existential restriction modifier
Autosomal dominant excess of transthyretin Is a True Thyroxine transport defect Inferred relationship Existential restriction modifier
X-linked variant form of thyroxine-binding globulin Is a True Thyroxine transport defect Inferred relationship Existential restriction modifier
Thyroxine plasma membrane transport defect Is a True Thyroxine transport defect Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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