237937008: Deficiency of Cobalamin E (disorder)

SNOMED CT Concept\Clinical finding\Disease\Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of sulfur-bearing amino acid metabolism\Functional defects of methionine synthase\Deficiency of Cobalamin E

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

Descriptions:

Id Description Lang Type Status Case? Module

356611010 Cobalamin E en Synonym Inactive Only initial character case insensitive SNOMED CT core module
626741010 Cobalamin E (disorder) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
3029263018 Deficiency of Cobalamin E (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3029367015 Deficiency of Cobalamin E en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets