Overview
16p13.11 microduplication syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Childhood attention deficit/hyperactivity disorder
Frequent (30-79%)HP:0007018
Language impairment
Frequent (30-79%)HP:0002463
Ligamentous laxity
Frequent (30-79%)HP:0001382
Mental and motor retardation
Frequent (30-79%)HP:0001263
Mental-retardation
Frequent (30-79%)HP:0001249
Polydactyly of the hand
Frequent (30-79%)HP:0001161
Aortic coarctation
Occasional (5-29%)HP:0001680
Arachnodactyly
Occasional (5-29%)HP:0001166
Atria septal defect
Occasional (5-29%)HP:0001631
Autism
Occasional (5-29%)HP:0000717
Craniosyostosis
Occasional (5-29%)HP:0001363
Dropped arches
Occasional (5-29%)HP:0001763
Pectus excavatum
Occasional (5-29%)HP:0000767
physical aggression
Occasional (5-29%)HP:0000718
Schizophrenia
Occasional (5-29%)HP:0100753
Tetrology of fallot
Occasional (5-29%)HP:0001636
Transposition of great vessels
Occasional (5-29%)HP:0001669
Turridolichocephaly
Occasional (5-29%)HP:0000268
VSD
Occasional (5-29%)HP:0001629
Quick Facts
- SNOMED CT
- 719578005
- UMLS CUI
- C4304595
- Fully Specified Name
- 16p13.11 microduplication syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 19
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.