Intraosseous hemangioma

disorder

SNOMED 764100007CUI C1847197

Overview

Intraosseous hemangioma 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.

Bleeding gums

Always present (100%)HP:0000225

Ectopic tooth eruption

Always present (100%)HP:4000093

Gap between large left and right abdominal muscles

Always present (100%)HP:0001540

Hypochromic anemia

Always present (100%)HP:0001931

Supraumbilical raphe

Always present (100%)HP:0410276

Unbalanced face

Always present (100%)HP:0000324

Anterior bulging of the globe of eye

Very frequent (80-99%)HP:0000520

Elevated alkaline phosphatase

Very frequent (80-99%)HP:0003155

Umbilical hernia

Very frequent (80-99%)HP:0001537

Visual loss

Very frequent (80-99%)HP:0000572

Intracranial hypertension

Frequent (30-79%)HP:0002516

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Cardiovascular system hereditary disorder(parent)

Infantile haemangioma of rare localisation(parent)

Congenital hemangioma(parent)

Quick Facts

SNOMED CT: 764100007
UMLS CUI: C1847197
Fully Specified Name: Primary intraosseous venous malformation (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 11

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.