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37695001: Neonatal hypermethioninemia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module Reference Sets
62873019 Neonatal hypermethioninemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core US English: Preferred (foundation metadata concept)
486786014 Neonatal hypermethioninaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
769591013 Neonatal hypermethioninemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)

0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal hypermethioninemia Is a Hypermethioninemia true Inferred relationship Some
Neonatal hypermethioninemia Finding site Body system structure false Inferred relationship Some
Neonatal hypermethioninemia Occurrence Congenital false Inferred relationship Some
Neonatal hypermethioninemia Is a Neonatal disorder false Inferred relationship Some
Neonatal hypermethioninemia Is a Neonatal metabolic disorder (disorder) true Inferred relationship Some
Neonatal hypermethioninemia Occurrence Neonatal true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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