361094004: Deficiency of tyraminase (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of tyraminase

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

477266014 Deficiency of monoamine oxidase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

477267017 Deficiency of tyraminase en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

742047012 Deficiency of tyraminase (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5227501000241111 déficit en tyraminase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Deficiency of tyraminase	Is a	Specific enzyme deficiency	true	Inferred relationship	Some
Deficiency of tyraminase	Finding site	Body system structure	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Monoamine oxidase-A deficiency is a very rare recessive X-linked biogenic amine metabolism disorder characterized clinically by mild intellectual deficit, impulsive aggressiveness, and sometimes violent behavior and presenting from childhood.	Is a	True	Deficiency of tyraminase	Inferred relationship	Some

This concept is not in any reference sets