Hereditary factor XI deficiency disease

disorder

SNOMED 49762007CUI C0015523

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormality of the intrinsic pathway

Very frequent (80-99%)HP:0010989

Bleeding tendency

Very frequent (80-99%)HP:0001892

Prolonged activated partial thromboplastin time

Very frequent (80-99%)HP:0003645

Prolonged bleeding after dental extraction

Very frequent (80-99%)HP:0006298

Frequent nosebleeds

Frequent (30-79%)HP:0000421

Hypermenorrhea

Frequent (30-79%)HP:0000132

Gastrointestinal haemorrhage

Very rare (1-4%)HP:0002239

Joint hemorrhage

Very rare (1-4%)HP:0005261

Factor XI deficiency

HP:0001929

Related Conditions

Factor XI deficiency, type II(child)

Factor XI deficiency, type III(child)

Factor XI deficiency, type I(child)

Recessive hereditary disorder (autosomal)(parent)

Contact factor deficiency(parent)

Hemophilia(parent)

Congenital disease(parent)

Factor XI deficiency(parent)

Quick Facts

SNOMED CT: 49762007
UMLS CUI: C0015523
Fully Specified Name: Hereditary factor XI 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.