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783773000: Congenital abnormal number of ostium of coronary artery (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5408656011 A rare, congenital, non-syndromic heart malformation characterized by more or less than one coronary ostium at the left and at the right aortic sinus of Valsalva. It may be asymptomatic or it leads to myocardial ischemia and technical difficulties during coronary angiography. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5408657019 A rare, congenital, non-syndromic heart malformation characterised by more or less than one coronary ostium at the left and at the right aortic sinus of Valsalva. It may be asymptomatic or it leads to myocardial ischaemia and technical difficulties during coronary angiography. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3760313013 Congenital abnormal number of coronary ostia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3760317014 Congenital abnormal number of ostium of coronary artery en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3760318016 Congenital abnormal number of ostium of coronary artery (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5856741000241111 anomalie congénitale du nombre d'ostium coronaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3390081001000113 Koronarostium, abnormale Anzahl de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare, congenital, non-syndromic heart malformation characterized by more or less than one coronary ostium at the left and at the right aortic sinus of Valsalva. It may be asymptomatic or it leads to myocardial ischemia and technical difficulties during coronary angiography. Is a Congenital anomaly of coronary artery true Inferred relationship Some
A rare, congenital, non-syndromic heart malformation characterized by more or less than one coronary ostium at the left and at the right aortic sinus of Valsalva. It may be asymptomatic or it leads to myocardial ischemia and technical difficulties during coronary angiography. Is a Abnormal ostium of coronary artery true Inferred relationship Some
A rare, congenital, non-syndromic heart malformation characterized by more or less than one coronary ostium at the left and at the right aortic sinus of Valsalva. It may be asymptomatic or it leads to myocardial ischemia and technical difficulties during coronary angiography. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
A rare, congenital, non-syndromic heart malformation characterized by more or less than one coronary ostium at the left and at the right aortic sinus of Valsalva. It may be asymptomatic or it leads to myocardial ischemia and technical difficulties during coronary angiography. Finding site Structure of ostium of coronary artery true Inferred relationship Some 1
A rare, congenital, non-syndromic heart malformation characterized by more or less than one coronary ostium at the left and at the right aortic sinus of Valsalva. It may be asymptomatic or it leads to myocardial ischemia and technical difficulties during coronary angiography. Associated morphology Congenital abnormal number false Inferred relationship Some 1
A rare, congenital, non-syndromic heart malformation characterized by more or less than one coronary ostium at the left and at the right aortic sinus of Valsalva. It may be asymptomatic or it leads to myocardial ischemia and technical difficulties during coronary angiography. Occurrence Congenital true Inferred relationship Some 1
A rare, congenital, non-syndromic heart malformation characterized by more or less than one coronary ostium at the left and at the right aortic sinus of Valsalva. It may be asymptomatic or it leads to myocardial ischemia and technical difficulties during coronary angiography. Associated morphology Abnormal number (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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