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718210003: Deficiency of monoamine oxidase A (disorder)

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3308700019 Deficiency of monoamine oxidase A (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3310405019 Deficiency of monoamine oxidase A en Synonym Active Initial character case insensitive SNOMED CT core
3311514018 Monoamine oxidase A deficiency en Synonym Active Initial character case insensitive SNOMED CT core
3311515017 Brunner syndrome en Synonym Active Case sensitive SNOMED CT core
3311518015 A very rare recessive X-linked biogenic amine metabolism disorder with clinical characteristics of mild intellectual deficit, impulsive aggressiveness, sometimes violent behavior and presenting from childhood. en Definition Active Case sensitive SNOMED CT core
3311519011 A very rare recessive X-linked biogenic amine metabolism disorder with clinical characteristics of mild intellectual deficit, impulsive aggressiveness, sometimes violent behaviour and presenting from childhood. en Definition Active Case sensitive SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Brunner syndrome	Is a	X-linked recessive hereditary disease	true	Inferred relationship	Some
Brunner syndrome	Is a	Inherited metabolic disorder of nervous system	true	Inferred relationship	Some
Brunner syndrome	Is a	X-linked hereditary disease	false	Inferred relationship	Some
Brunner syndrome	Is a	Deficiency of tyraminase	true	Inferred relationship	Some
Brunner syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Brunner syndrome	Finding site	Structure of nervous system	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Id	Description	Lang	Type	Status	Case?	Module
3308700019	Deficiency of monoamine oxidase A (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3310405019	Deficiency of monoamine oxidase A	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3311514018	Monoamine oxidase A deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3311515017	Brunner syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3311518015	A very rare recessive X-linked biogenic amine metabolism disorder with clinical characteristics of mild intellectual deficit, impulsive aggressiveness, sometimes violent behavior and presenting from childhood.	en	Definition	Active	Case sensitive	SNOMED CT core
3311519011	A very rare recessive X-linked biogenic amine metabolism disorder with clinical characteristics of mild intellectual deficit, impulsive aggressiveness, sometimes violent behaviour and presenting from childhood.	en	Definition	Active	Case sensitive	SNOMED CT core