66185005: Autosomal dominant excess of transthyretin (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of head and neck region\Finding of neck region\...
• \Finding of thyroid gland\Thyroid disease\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant excess of transthyretin
• \Disorder of neck\Thyroid disease\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant excess of transthyretin
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant excess of transthyretin
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant excess of transthyretin
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant excess of transthyretin
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant excess of transthyretin
• \Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant excess of transthyretin
• \Disease\Disorder of body system\Disorder of endocrine system\Thyroid disease\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant excess of transthyretin
• \Disease\Disorder of neck\Thyroid disease\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant excess of transthyretin
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant excess of transthyretin
• \Disease\Congenital disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant excess of transthyretin

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
109907014	Autosomal dominant excess of transthyretin	en	Synonym	Active	Case insensitive	SNOMED CT core
2647247015	Autosomal dominant excess of thyroxine-binding prealbumin	en	Synonym	Active	Case insensitive	SNOMED CT core
805770015	Autosomal dominant excess of transthyretin (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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