FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

703221003: Congenital intracranial vascular malformation (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3007695013 Intracranial vascular malformation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3007755015 Congenital intracranial vascular malformation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3007774011 Congenital intracranial vascular malformation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3007695013 Intracranial vascular malformation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3007695013 Intracranial vascular malformation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3007755015 Congenital intracranial vascular malformation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3007755015 Congenital intracranial vascular malformation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3007774011 Congenital intracranial vascular malformation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3007774011 Congenital intracranial vascular malformation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5450801000241110 malformation vasculaire intracrânienne congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5450801000241110 malformation vasculaire intracrânienne congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


23 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital intracranial vascular malformation (disorder) Is a Congenital anomaly of head true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital intracranial vascular malformation (disorder) Is a Intracerebral vascular finding true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital intracranial vascular malformation (disorder) Is a Congenital anomaly of cerebrovascular system true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital intracranial vascular malformation (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital intracranial vascular malformation (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital intracranial vascular malformation (disorder) Finding site Intracranial vascular structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital intracranial vascular malformation (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital intracranial vascular malformation (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital intracranial vascular malformation (disorder) Is a Congenital vascular malformation (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital anomaly of cerebral artery Is a True Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital arteriovenous fistula of brain Is a True Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Vein of Galen malformation (disorder) Is a True Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebral arteriovenous aneurysm (disorder) Is a True Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital malformation of dural sinus (disorder) Is a True Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cerebral arteriovenous malformation (disorder) Is a True Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Bregeat's syndrome Is a False Congenital intracranial vascular malformation (disorder) 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 Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aneurysm of anterior communicating artery Is a True Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dural carotid cavernous fistula (disorder) Is a False Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary neurocutaneous angiomata (disorder) Is a False Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cavernous hemangioma of brain (disorder) Is a False Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital fenestration of basilar artery Is a True Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital duplication of anterior communicating artery (disorder) Is a True Congenital intracranial vascular malformation (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start