Loeys-Dietz syndrome

Caring for someone with this diagnosis? Eleplan keeps diagnoses, medications, documents and every specialist in one plan.

Start free with Eleplan

Loeys-Dietz syndrome

ORPHA:60030Malformation syndrome

Also called Aortic aneurysm syndrome due to TGF-beta receptors anomalies

What it is

Loeys-Dietz syndrome is a rare genetic connective tissue disorder characterized by a broad spectrum of craniofacial, vascular and skeletal manifestations with four genetic subtypes described forming a clinical continuum.

Key facts

Age of onset
Antenatal, Infancy, Neonatal
Inheritance
Autosomal dominant, Autosomal recessive
Classified as
Malformation syndrome

Signs and symptoms

These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.

Genes

IPO8Disease-causing germline mutation(s) (loss of function)
SMAD2Disease-causing germline mutation(s)
SMAD3Disease-causing germline mutation(s)
TGFB2Disease-causing germline mutation(s)
TGFB3Disease-causing germline mutation(s)
TGFBR1Disease-causing germline mutation(s)
TGFBR2Disease-causing germline mutation(s)

ICD-10 codes

Q87.4filed under a broader ICD-10 category — shared with 5 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

GARD 10788MEDDRA 10081284MESH D055947MONDO 0018954OMIM 609192OMIM 610168OMIM 613795OMIM 614816OMIM 615582OMIM 619472OMIM 619656UMLS C2697932

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

Powered by Eleplan

A rare diagnosis is just the start. Eleplan keeps the whole care plan in one place.

Diagnoses, medications, documents, appointments, and the whole care team — organized and always in sync, so you are not retelling the same story to every new specialist. With Ellie, your AI care assistant, on top of it. Free to start.