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37695001: Neonatal hypermethioninemia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
62873019 Neonatal hypermethioninemia en Synonym Active Entire term case insensitive SNOMED CT core module
486786014 Neonatal hypermethioninaemia en Synonym Active Entire term case insensitive SNOMED CT core module
769591013 Neonatal hypermethioninemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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