73068003: X-linked variant form of thyroxine-binding globulin (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\X-linked variant form of thyroxine-binding globulin
• \Finding of neck region\Disease of neck\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\X-linked variant form of thyroxine-binding globulin
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\X-linked variant form of thyroxine-binding globulin
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\X-linked variant form of thyroxine-binding globulin
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder (disorder)\X-linked hereditary disease\X-linked variant form of thyroxine-binding globulin
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\X-linked variant form of thyroxine-binding globulin
• \Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\X-linked variant form of thyroxine-binding globulin
• \Disease\Disorder of body system\Disorder of endocrine system (disorder)\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\X-linked variant form of thyroxine-binding globulin
• \Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\X-linked variant form of thyroxine-binding globulin
• \Disease\Disease of neck\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\X-linked variant form of thyroxine-binding globulin
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\X-linked variant form of thyroxine-binding globulin

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
121364017	X-linked variant form of thyroxine-binding globulin	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
813415013	X-linked variant form of thyroxine-binding globulin (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
121364017	X-linked variant form of thyroxine-binding globulin	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
813415013	X-linked variant form of thyroxine-binding globulin (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
813415013	X-linked variant form of thyroxine-binding globulin (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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