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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\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant variant form of albumin

\Disorder of neck\Disorder of thyroid gland\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\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Autosomal dominant variant form of albumin
\Disease\Disorder of neck\Disorder of thyroid gland\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, 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

35885010 Autosomal dominant variant form of albumin en Synonym Active Entire term case insensitive SNOMED CT core module

750653014 Autosomal dominant variant form of albumin (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal dominant variant form of albumin	Is a	Thyroxine transport defect	true	Inferred relationship	Existential restriction modifier
Autosomal dominant variant form of albumin	Is a	Reproductive system hereditary disorder	false	Inferred relationship	Existential restriction modifier
Autosomal dominant variant form of albumin	Is a	Hereditary disorder of endocrine system	false	Inferred relationship	Existential restriction modifier
Autosomal dominant variant form of albumin	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Autosomal dominant variant form of albumin	Finding site	Entire endocrine gonad	false	Inferred relationship	Existential restriction modifier
Autosomal dominant variant form of albumin	Interprets	Biological transport, function	false	Inferred relationship	Existential restriction modifier
Autosomal dominant variant form of albumin	Finding site	Thyroid structure	false	Inferred relationship	Existential restriction modifier
Autosomal dominant variant form of albumin	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Autosomal dominant variant form of albumin	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Autosomal dominant variant form of albumin	Finding site	Thyroid structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
35885010	Autosomal dominant variant form of albumin	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
750653014	Autosomal dominant variant form of albumin (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module