Preferred Name

Cerebral arteriovenous malformation

ID

http://www.orpha.net/ORDO/Orphanet_46724

alternative_term

Intracranial arteriovenous malformation

definition

Cerebral arteriovenous malformation (AVM) is a congenital malformative communication between the veins and the arteries in the brain in the form of a nidus, an anatomical structure composed of dilated and tangled supplying arterioles and drainage veins with no intervening capillary bed, that can be asymptomatic or cause, depending on the location and the size of the AVM, headaches of varying severity, generalized or focal seizures, focalneurological defects (weakness, numbness, speech difficulties, vision loss) or potentially fatal intracranial hemorrhage in case the AVM ruptures.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=46724

has_age_of_onset

All ages

has_inheritance

No data available

hasDbXref

ICD-11:8B22.40

MeSH:D002538

ICD-10:Q28.2

UMLS:C0917804

OMIM:108010

label

Cerebral arteriovenous malformation

notation

ORPHA:46724

part_of

http://www.orpha.net/ORDO/Orphanet_211266

http://www.orpha.net/ORDO/Orphanet_371436

http://www.orpha.net/ORDO/Orphanet_211240

http://www.orpha.net/ORDO/Orphanet_102006

prefixIRI

ORDO:Orphanet_46724

prefLabel

Cerebral arteriovenous malformation

present_in

Europe AND has_point_prevalence_average_value : 6.0 AND has_point_prevalence_range : 1-9 / 100 000

treeView

http://www.orpha.net/ORDO/Orphanet_211266

http://www.orpha.net/ORDO/Orphanet_371436

http://www.orpha.net/ORDO/Orphanet_211240

http://www.orpha.net/ORDO/Orphanet_102006

subClassOf

http://www.orpha.net/ORDO/Orphanet_377791

http://www.orpha.net/ORDO/Orphanet_557493

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Delete Mapping To Ontology Source
http://www.orpha.net/ORDO/Orphanet_46724 Experimental Factor Ontology / 实验性因素本体 LOOM
http://www.orpha.net/ORDO/Orphanet_46724 Experimental Factor Ontology / 实验性因素本体 SAME_URI
http://purl.obolibrary.org/obo/HP_0002408 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU000095 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM