Trisomy X syndrome

disorder

SNOMED 35111009CUI C0221033

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormality of chromosome segregation

Very frequent (80-99%)HP:0002916

Accelerated linear growth

Frequent (30-79%)HP:0000098

Cognitive delay

Frequent (30-79%)HP:0001263

Constipation

Frequent (30-79%)HP:0002019

Delayed language development

Frequent (30-79%)HP:0000750

Hypotonia, early

Frequent (30-79%)HP:0008947

Intellectual impairment

Frequent (30-79%)HP:0100543

No development of motor milestones

Frequent (30-79%)HP:0001270

Palpebronasal fold

Frequent (30-79%)HP:0000286

Permanent curving of the pinkie finger

Frequent (30-79%)HP:0004209

Specific learning disability

Frequent (30-79%)HP:0001328

Upset stomach

Frequent (30-79%)HP:0002027

Anxiety disease

Occasional (5-29%)HP:0000739

Atria septal defect

Occasional (5-29%)HP:0001631

Autoimmune disorder

Occasional (5-29%)HP:0002960

Childhood attention deficit/hyperactivity disorder

Occasional (5-29%)HP:0007018

Depressive episode

Occasional (5-29%)HP:0000716

Developmental dysplasia of the hip

Occasional (5-29%)HP:0001385

Increased distance between eyes

Occasional (5-29%)HP:0000316

Joint ligamentous laxity

Occasional (5-29%)HP:0001382

Mongoloid slant

Occasional (5-29%)HP:0000582

Multicystic kidney dysplasia

Occasional (5-29%)HP:0000003

Nonprogressive mental retardation

Occasional (5-29%)HP:0001249

Pectus excavatum

Occasional (5-29%)HP:0000767

Premature menopause

Occasional (5-29%)HP:0008209

Previous menstrual periods stop

Occasional (5-29%)HP:0000869

Renal hypoplasia/aplasia

Occasional (5-29%)HP:0008678

Seizures

Occasional (5-29%)HP:0001250

Tremor

Occasional (5-29%)HP:0001337

VSD

Occasional (5-29%)HP:0001629

Related Conditions

Sex chromosome abnormality - female phenotype(parent)

Anomaly of chromosome X(parent)

Quick Facts

SNOMED CT: 35111009
UMLS CUI: C0221033
Fully Specified Name: Trisomy X syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.