Factor IX deficiency

disorder

SNOMED 767712006CUI C0008533

Overview

Factor IX deficiency is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Treatments & Interventions

Coagulation factor VII

substance

Coagulation factor IX

substance

Anti-inhibitor coagulant complex

substance

Recombinant coagulation factor IX

substance

Nonacog alfa

substance

Albutrepenonacog alfa

substance

Nonacog beta pegol

substance

Signs & Symptoms

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

Blood in urine

Very frequent (80-99%)HP:0000790

Bruising susceptibility

Very frequent (80-99%)HP:0000978

Cephalohematoma

Very frequent (80-99%)HP:0012541

Delayed onset bleeding

Very frequent (80-99%)HP:0040232

Excessive bleeding after minor trauma

Very frequent (80-99%)HP:0001934

Increased bleeding time

Very frequent (80-99%)HP:0003010

Intracranial haemorrhage

Very frequent (80-99%)HP:0002170

Intramuscular haematoma

Very frequent (80-99%)HP:0012233

Joint hemorrhage

Very frequent (80-99%)HP:0005261

Menometrorrhagia

Very frequent (80-99%)HP:0400008

Poor wound healing

Very frequent (80-99%)HP:0001058

Prolonged activated partial thromboplastin time

Very frequent (80-99%)HP:0003645

Prolonged bleeding after dental extraction

Very frequent (80-99%)HP:0006298

Protracted bleeding after surgery

Very frequent (80-99%)HP:0004846

Reduced factor IX activity

Very frequent (80-99%)HP:0011858

Spontaneous, recurrent nosebleed

Very frequent (80-99%)HP:0004406

Black faeces

Occasional (5-29%)HP:0002249

Hematemesis

Occasional (5-29%)HP:0002248

Nasal hemorrhage

Occasional (5-29%)HP:0000421

Petechiae

Occasional (5-29%)HP:0000967

Gastrointestinal haemorrhage

HP:0002239

Low factor II activity

Excluded (<1%)HP:0008151

Osteoarthritis

HP:0002758

Prolonged whole-blood clotting time

HP:0005542

Related Conditions

Hemophilia B(child)

Acquired factor IX deficiency disease(child)

Coagulation factor deficiency syndrome(parent)

Quick Facts

SNOMED CT: 767712006
UMLS CUI: C0008533
Fully Specified Name: Factor IX deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 24
Known Treatments: 7

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.