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721187005: 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
903431000172110 déficit en méthylcobalamine type cblG fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
925341000172119 déficit fonctionnel en méthionine synthase type cblG fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
883291000172118 functionele methioninesynthasedeficiëntie type cblG nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
916771000172112 methylcobalaminedeficiëntie type cblG nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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