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360376008: Functional defects of methionine synthase (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
476118018 Functional defects of methionine synthase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
740096014 Functional defects of methionine synthase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Functional defects of methionine synthase est un(e) (attribut) Disorder of sulphur-bearing amino acid metabolism true Inferred relationship Some
Functional defects of methionine synthase localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Functional defects of methionine synthase survenue (attribut) congénital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Deficiency of Cobalamin E (disorder) est un(e) (attribut) True Functional defects of methionine synthase Inferred relationship Some
Deficiency of Cobalamin G (disorder) est un(e) (attribut) True Functional defects of methionine synthase Inferred relationship Some
Homocystinuria without methylmalonic aciduria (disorder) est un(e) (attribut) True Functional defects of methionine synthase Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

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