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IPCCC ICD-11 Congenital Heart Atlas

You are here: Hypoplasia of aortic arch Congenital anomaly of aortic arch Congenital anomaly of aorta or its branches Congenital anomaly of great arteries including arterial duct Structural developmental anomaly of heart or great vessels

IPCCC Term Hypoplasia of aortic arch
IPCCC Code 09.29.11
ICD-11 MMS LA8B.2Y
ICD-11 Code 2084361271

Definition

A congenital cardiovascular malformation in which there is diffuse luminal narrowing of the aortic arch (below the lower limit of normal adjusted for body size).

Synonyms/Abbreviations

Hypoplastic aortic arch, Arch hypoplasia, Aortic hypoplasia; Aortic arch hypoplasia

STS-EACTS-derived IPCCC term

Aortic arch hypoplasia

EPCC-derived IPCCC term

Aortic arch hypoplasia

ICD-11 MMS code or crossmap

LA8B.2Y*: TLA8B.1*: This Foundation term is not in ICD-11 MMS. If using MMS to code, crossmap to "Other specified congenital anomaly of aorta or its branches" with code LA8B.2Y

ICD-10 MMS code or crossmap

Q25.4**: This Foundation term is not in ICD-10. Crossmap to "Other congenital malformations of aorta" with code Q25.4

Parent

Congenital anomaly of aortic arch

Siblings

Coding Notes

Hypoplasia of the aortic arch is hypoplasia of the proximal or distal transverse arch or the aortic isthmus. The isthmus (arch between the left subclavian and insertion of the patent ductus arteriosus / ligamentum arteriosum) is hypoplastic if its diameter is less than 40% of the diameter of the ascending aorta. The proximal transverse arch (arch between the innominate and left carotid arteries) and distal transverse arch (arch between the left carotid and left subclavian arteries) are hypoplastic if their diameters are less than 60% and 50%, respectively, of the diameter of the ascending aorta.

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