21367009: Autosomal dominant variant form of albumin (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 variant form of albumin
• \Disorder of neck\Thyroid disease\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant variant form of albumin
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant variant form of albumin
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant variant form of albumin
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant variant form of albumin
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant variant form of albumin
• \Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant variant form of albumin
• \Disease\Disorder of body system\Disorder of endocrine system\Thyroid disease\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant variant form of albumin
• \Disease\Disorder of neck\Thyroid disease\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant variant form of albumin
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant variant form of albumin
• \Disease\Congenital disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant variant form of albumin

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
35885010	Autosomal dominant variant form of albumin	en	Synonym	Active	Case insensitive	SNOMED CT core
750653014	Autosomal dominant variant form of albumin (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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