Juvenile xanthogranuloma

disorder

SNOMED 400031009CUI C0043324

Overview

Juvenile xanthogranuloma 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 oral mucosa morphology

Occasional (5-29%)HP:0011830

Abnormality of the respiratory system

Occasional (5-29%)HP:0002086

Asymmetry of iris pigmentation

Occasional (5-29%)HP:0200064

Blepharitis

Occasional (5-29%)HP:0000498

Glaucoma

Occasional (5-29%)HP:0000501

Hyphema

Occasional (5-29%)HP:0011886

Iritis

Occasional (5-29%)HP:0001101

Multiple cafe-au-lait spots

Occasional (5-29%)HP:0007565

Myeloproliferative disorder

Occasional (5-29%)HP:0005547

Prominent eyes

Occasional (5-29%)HP:0000520

Uveitis

Occasional (5-29%)HP:0000554

Visual loss

Occasional (5-29%)HP:0000572

Related Conditions

Juvenile xanthogranuloma of skin(child)

Multiple eruptive juvenile xanthogranuloma(child)

Juvenile xanthogranuloma of iris(child)

Xanthogranuloma(parent)

Quick Facts

SNOMED CT: 400031009
UMLS CUI: C0043324
Fully Specified Name: Juvenile xanthogranuloma (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.