21367009: Autosomal dominant variant form of albumin (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)\Autosomal dominant variant form of albumin
\Finding of neck region\Disease of neck\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\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 (disorder)\Autosomal dominant variant form of albumin
\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)\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 foetus and/or newborn\Congenital disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
\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)\Autosomal dominant variant form of albumin
\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)\Autosomal dominant variant form of albumin
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
\Disease\Disease of neck\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect (disorder)\Autosomal dominant variant form of albumin

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

Descriptions:

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
35885010	Autosomal dominant variant form of albumin	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
750653014	Autosomal dominant variant form of albumin (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
35885010	Autosomal dominant variant form of albumin	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
35885010	Autosomal dominant variant form of albumin	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
750653014	Autosomal dominant variant form of albumin (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
750653014	Autosomal dominant variant form of albumin (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5786271000241119	forme variante de l'albumine autosomique dominante	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5786271000241119	forme variante de l'albumine autosomique dominante	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module