Emberger syndrome

disorder

SNOMED 700057001CUI C3279664

Overview

Emberger 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.

Lymphatic obstruction

Very frequent (80-99%)HP:0001004

Acute myeloid leukaemia

Frequent (30-79%)HP:0004808

Hypoplastic myelodysplasia

Frequent (30-79%)HP:0002863

Inverted CD4/CD8 ratio

Occasional (5-29%)HP:0033222

Long fingers

Occasional (5-29%)HP:0100807

Ocular hypotelorism

Occasional (5-29%)HP:0000601

Palpebronasal fold

Occasional (5-29%)HP:0000286

Pterygium colli

Occasional (5-29%)HP:0000465

Tapering fingers

Occasional (5-29%)HP:0001182

Warts

Occasional (5-29%)HP:0200043

Blood cancer

HP:0001909

Pancytopenia

HP:0001876

Skin infections

HP:0100658

Related Conditions

Hereditary neoplastic syndrome(parent)

Autosomal dominant hereditary disorder(parent)

Hereditary lymphedema(parent)

Hereditary disorder by system(parent)

Acute myeloid leukaemia with multilineage dysplasia(parent)

Quick Facts

SNOMED CT: 700057001
UMLS CUI: C3279664
Fully Specified Name: Emberger syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.