Overview
Trisomy 2 mosaicism 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.
Decreased amniotic fluid index
Frequent (30-79%)HP:0001562
Decreased size of cranium
Frequent (30-79%)HP:0000252
Delayed gross motor development
Frequent (30-79%)HP:0002194
Growth delay as children
Frequent (30-79%)HP:0008897
Hernia
Frequent (30-79%)HP:0100790
Hypotrophic midface
Frequent (30-79%)HP:0011800
Increased distance between eyes
Frequent (30-79%)HP:0000316
Intrauterine growth retardation, IUGR
Frequent (30-79%)HP:0001511
Abnormally small eyeball
Occasional (5-29%)HP:0000568
Aganglionic megacolon
Occasional (5-29%)HP:0002251
Cardiac anomaly
Occasional (5-29%)HP:0001627
Cleft lip
Occasional (5-29%)HP:0410030
Cleft of palate
Occasional (5-29%)HP:0000175
Dilated cerebral ventricle
Occasional (5-29%)HP:0002119
Intestinal malrotation
Occasional (5-29%)HP:0002566
Narrow cranium shape
Occasional (5-29%)HP:0000268
Neural tube defect
Occasional (5-29%)HP:0045005
Neurodevelopmental delay
Occasional (5-29%)HP:0012758
Preaxial hand polydactyly
Occasional (5-29%)HP:0001177
Scoliosis
Occasional (5-29%)HP:0002650
Short ulna
Occasional (5-29%)HP:0003022
Shortening of radius
Occasional (5-29%)HP:0002984
Split spine
Occasional (5-29%)HP:0002414
Thinning of the corpus callosum
Occasional (5-29%)HP:0033725
Quick Facts
- SNOMED CT
- 764623009
- UMLS CUI
- C4707010
- Fully Specified Name
- Mosaic trisomy 2 syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 24
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.