Trisomy 15 mosaicism

disorder

SNOMED 764619001CUI C2931707

Overview

Trisomy 15 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.

Abnormal hands

Very frequent (80-99%)HP:0001155

Brain and/or spinal cord issue

Very frequent (80-99%)HP:0000707

Central hypotonia

Very frequent (80-99%)HP:0001252

Abnormality of chromosome segregation

Frequent (30-79%)HP:0002916

Finger pointing in a different direction than usual

Frequent (30-79%)HP:0004097

Proximal interphalangeal finger joint contractures

Frequent (30-79%)HP:0100490

Related Conditions

Anomaly of chromosome pair 15(parent)

Trisomy and partial trisomy of autosome(parent)

Multiple system malformation syndrome(parent)

Quick Facts

SNOMED CT: 764619001
UMLS CUI: C2931707
Fully Specified Name: Mosaic trisomy 15 syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 6

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.