Overview
Microduplication Xp11.22p11.23 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.
Dull intelligence
Very frequent (80-99%)HP:0001249
Speech delay
Very frequent (80-99%)HP:0000750
EEG with centrotemporal focal spike waves
Frequent (30-79%)HP:0012557
Fallen arches
Frequent (30-79%)HP:0001763
Husky voice
Frequent (30-79%)HP:0001609
Nasal speech
Frequent (30-79%)HP:0001611
Obesity
Frequent (30-79%)HP:0001513
Pes cavus
Frequent (30-79%)HP:0001761
Precocious puberty
Frequent (30-79%)HP:0000826
Seizures
Frequent (30-79%)HP:0001250
Syndactyly of feet
Frequent (30-79%)HP:0001770
Autism
Occasional (5-29%)HP:0000717
Quick Facts
- SNOMED CT
- 721881008
- UMLS CUI
- C4303068
- Fully Specified Name
- Microduplication Xp11.22p11.23 syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 12
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.