721187005: déficit en méthylcobalamine type cblG (trouble)

SNOMED CT Concept\constatation clinique\Disease\...

\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Homocystinuria without methylmalonic aciduria (disorder)\Methylcobalamin deficiency type cbl G (disorder)

\trouble métabolique\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of sulphur-bearing amino acid metabolism\...

\Functional defects of methionine synthase\Homocystinuria without methylmalonic aciduria (disorder)\Methylcobalamin deficiency type cbl G (disorder)

\Homocystinuria\Homocystinuria without methylmalonic aciduria (disorder)\Methylcobalamin deficiency type cbl G (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3324559012 Methylcobalamin deficiency type cbl G (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3324560019 Methylcobalamin deficiency type cbl G en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

757031000241117 déficit en méthylcobalamine type cblG (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

903431000172110 déficit en méthylcobalamine type cblG fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

925341000172119 déficit fonctionnel en méthionine synthase type cblG fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Methylcobalamin deficiency type cbl G (disorder)	est un(e) (attribut)	Homocystinuria without methylmalonic aciduria (disorder)	true	Inferred relationship	Some

Inbound Relationships

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Active

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Characteristic

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Group

Reference Sets

Canada English language reference set (foundation metadata concept)