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37695001: Neonatal hypermethioninemia (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of neonate\Neonatal disorder\Neonatal metabolic disorder (disorder)\Neonatal hypermethioninemia

\Disease\Disorder of foetus and/or newborn\Neonatal disorder\Neonatal metabolic disorder (disorder)\Neonatal hypermethioninemia
\Disease\Metabolic disease\Neonatal metabolic disorder (disorder)\Neonatal hypermethioninemia
\Disease\Metabolic disease\Disorder of organic acid metabolism (disorder)\Disorder of amino acid metabolism (disorder)\Disorder of amino acid and organic acid metabolism\Disorder of sulphur-bearing amino acid metabolism\Hypermethioninaemia\Neonatal hypermethioninemia

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Neonatal hypermethioninemia	Is a	Hypermethioninaemia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Neonatal hypermethioninemia	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Neonatal hypermethioninemia	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Neonatal hypermethioninemia	Is a	Neonatal disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Neonatal hypermethioninemia	Occurrence	Neonatal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Neonatal hypermethioninemia	Is a	Neonatal metabolic disorder (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

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
62873019	Neonatal hypermethioninemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
486786014	Neonatal hypermethioninaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
769591013	Neonatal hypermethioninemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
62873019	Neonatal hypermethioninemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
62873019	Neonatal hypermethioninemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
486786014	Neonatal hypermethioninaemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
486786014	Neonatal hypermethioninaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
769591013	Neonatal hypermethioninemia (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
769591013	Neonatal hypermethioninemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4512761000241114	hyperméthioninémie néonatale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4512761000241114	hyperméthioninémie néonatale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module