Factor XII deficiency disease

disorder

SNOMED 46981006CUI C0015526

Overview

Factor XII deficiency disease 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.

Factor XII deficiency

Very frequent (80-99%)HP:0004841

Prolonged activated partial thromboplastin time

Very frequent (80-99%)HP:0003645

Abnormal thrombosis

Occasional (5-29%)HP:0001977

Embolism and thrombosis

Occasional (5-29%)HP:0001907

Retinal arteriolar occlusion

Occasional (5-29%)HP:0007985

Retinal vein occlusion

Occasional (5-29%)HP:0012636

Bleeding tendency

Very rare (1-4%)HP:0001892

Penetrating foot ulcers

Very rare (1-4%)HP:0001026

Prolonged whole-blood clotting time

HP:0005542

Related Conditions

Acquired factor XII deficiency disease(child)

Hereditary factor XII deficiency disease(child)

Contact factor deficiency(parent)

Coagulation factor deficiency syndrome(parent)

Quick Facts

SNOMED CT: 46981006
UMLS CUI: C0015526
Fully Specified Name: Factor XII deficiency disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.