69116000: Moyamoya disease (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Disorder of brain\Moyamoya disease
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Moyamoya disease

\Central nervous system finding\Finding of brain\Disorder of brain\Moyamoya disease
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Moyamoya disease

\Cardiovascular finding\Disorder of cardiovascular system\Cerebrovascular disease (disorder)\Moyamoya disease

\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Moyamoya disease
\Disease\Disorder of body system\Disorder of cardiovascular system\Cerebrovascular disease (disorder)\Moyamoya disease
\Disease\Disorder of head (disorder)\Disorder of brain\Moyamoya disease

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

114794013 Moyamoya disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

809026012 Moyamoya disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

114794013 Moyamoya disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

809026012 Moyamoya disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

809026012 Moyamoya disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

3427911001000117 Moyamoya-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

205161000172112 maladie de Moya-Moya fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

205161000172112 maladie de Moya-Moya fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3427911001000117 Moyamoya-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Moyamoya disease	Is a	Disorder of artery of neck	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Moyamoya disease	Is a	Cerebral arteritis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Moyamoya disease	Finding site	Structure of intracranial artery	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Moyamoya disease	Associated morphology	inflammation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Moyamoya disease	Finding site	Carotid artery structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Moyamoya disease	Is a	Cerebrovascular disease (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Moyamoya disease	Finding site	Cerebrovascular system structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Moyamoya disease	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Moyamoya disease	Is a	Disorder of soft tissue of body cavity	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Moyamoya disease	Is a	Disorder of brain	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Moyamoya disease with early-onset achalasia is an exceedingly rare autosomal recessive neurological disorder reported only in a few families so far. It is characterized by the association of early onset achalasia (manifesting in infancy) with severe intracranial angiopathy that is consistent with moyamoya angiopathy in most cases. Other variable associated manifestations include hypertension, Raynaud phenomenon, and livedo reticularis.	Is a	True	Moyamoya disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Moyamoya angiopathy - short stature - facial dysmorphism - hypergonadotropic hypogonadism is a very rare, hereditary, neurological, dysmorphic syndrome characterized by moyamoya disease, short stature of postnatal onset, and stereotyped facial dysmorphism.	Is a	True	Moyamoya disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Secondary moyamoya disease	Is a	True	Moyamoya disease	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets