Four X syndrome

disorder

SNOMED 10567003CUI C0265496

Overview

Four X 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.

Cognitive deficits

Frequent (30-79%)HP:0100543

Fused forearm bones

Frequent (30-79%)HP:0002974

Increased distance between eyes

Frequent (30-79%)HP:0000316

Joint instability

Frequent (30-79%)HP:0001382

Mongoloid slant

Frequent (30-79%)HP:0000582

Palpebronasal fold

Frequent (30-79%)HP:0000286

Peripheral hypotonia

Frequent (30-79%)HP:0001252

Psychomotor development deficiency

Frequent (30-79%)HP:0001263

Specific learning disability

Frequent (30-79%)HP:0001328

Squint

Frequent (30-79%)HP:0000486

Tooth abnormalities

Frequent (30-79%)HP:0000164

Abnormality of cardiovascular system morphology

Occasional (5-29%)HP:0030680

Abnormality of immune system physiology

Occasional (5-29%)HP:0010978

Brachydactyly

Occasional (5-29%)HP:0001156

Curvature of little finger

Occasional (5-29%)HP:0004209

Developmental dysplasia of the hip

Occasional (5-29%)HP:0001385

Related Conditions

Female with more than three X chromosomes(parent)

Anomaly of chromosome X(parent)

Multiple malformation syndrome with facial defects as major feature(parent)

Sex chromosome aneuploidy(parent)

Quick Facts

SNOMED CT: 10567003
UMLS CUI: C0265496
Fully Specified Name: Tetrasomy X syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 16

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.