237937008: Deficiency of Cobalamin E (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Metabolic disease\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\Deficiency of Cobalamin E (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

3029263018 Deficiency of Cobalamin E (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3029367015 Deficiency of Cobalamin E en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

975171000052117 kobalamin E sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Deficiency of Cobalamin E (disorder)	Is a	Functional defects of methionine synthase	true	Inferred relationship	Some
Deficiency of Cobalamin E (disorder)	Finding site	Body system structure	false	Inferred relationship	Some
Deficiency of Cobalamin E (disorder)	Occurrence	Congenital	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets