Winship Viljoen Leary syndrome

disorder

SNOMED 719380003CUI C1855080

Overview

Winship Viljoen Leary 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

Very frequent (80-99%)HP:0100543

Decreased size of cranium

Very frequent (80-99%)HP:0000252

Poor school performance

Very frequent (80-99%)HP:0001249

Stretched and thinned heart muscle

Very frequent (80-99%)HP:0001644

Abnormality of the auricle

Frequent (30-79%)HP:0000356

Curvature of little finger

Frequent (30-79%)HP:0004209

Decreased body height

Frequent (30-79%)HP:0004322

Space between great toe and second toe

Frequent (30-79%)HP:0001852

Dilated cerebral ventricle

Occasional (5-29%)HP:0002119

Epilepsy

Occasional (5-29%)HP:0001250

Narrow, high-arched roof of mouth

Occasional (5-29%)HP:0002705

Retinal pigmentary anomaly

Occasional (5-29%)HP:0007703

Sloping forehead

Occasional (5-29%)HP:0000340

Small for gestational age infant

Occasional (5-29%)HP:0001511

VSD

Occasional (5-29%)HP:0001629

Related Conditions

Multiple system malformation syndrome(parent)

Recessive hereditary disorder (autosomal)(parent)

Cardiovascular system hereditary disorder(parent)

Congestive cardiomyopathy(parent)

Developmental hereditary disorder(parent)

Congenital microcephalus(parent)

Genetic intellectual disability(parent)

Quick Facts

SNOMED CT: 719380003
UMLS CUI: C1855080
Fully Specified Name: Microcephalus cardiomyopathy syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.