Orphanet: Síndrome de microduplicación 3q29

Search for a rare disease

* (*) mandatory field

Other search option(s)

Suggest an update

(*) Required fields.


Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Captcha image

3q29 microduplication syndrome

Disease definition

3q29 microduplications are recently described chromosomal abnormalities with unclear clinical significance.


Classification level: Disorder
  • Synonym(s):
    • Trisomy 3q29
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant or Not applicable 
  • Age of onset: Infancy, Neonatal
  • ICD-10: Q92.3
  • OMIM: 611936
  • UMLS: C2749873
  • MeSH: -
  • GARD: 10360
  • MedDRA: -

Detailed information


The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.