← Back to Conditions

Factor X deficiency

disorder
SNOMED 76642003CUI C0015519

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.

Low factor II activity
Always present (100%)HP:0008151
Reduced factor X activity
Always present (100%)HP:0008321
Prolonged bleeding after dental extraction
Very frequent (80-99%)HP:0006298
Protracted bleeding after surgery
Very frequent (80-99%)HP:0004846
Frequent nosebleeds
Frequent (30-79%)HP:0000421
Abnormal umbilical stump bleeding
Occasional (5-29%)HP:0011884
Antepartum hemorrhage
Occasional (5-29%)HP:0025328
Bruising susceptibility
Occasional (5-29%)HP:0000978
Gastrointestinal haemorrhage
Occasional (5-29%)HP:0002239
High urine occult blood
Occasional (5-29%)HP:0000790
Hypermenorrhea
Occasional (5-29%)HP:0000132
Intramuscular haematoma
Occasional (5-29%)HP:0012233
Joint hemorrhage
Occasional (5-29%)HP:0005261
Oral cavity bleeding
Occasional (5-29%)HP:0030140
Post-partum hemorrhage
Occasional (5-29%)HP:0011891
Spontaneous hematomas
Occasional (5-29%)HP:0007420
Hematoperitoneum
Very rare (1-4%)HP:0011854
Subarachnoid hemorrhage
Very rare (1-4%)HP:0002138
Bleeding gums
HP:0000225
Intracranial haemorrhage
HP:0002170
Prolonged activated partial thromboplastin time
HP:0003645

Quick Facts

SNOMED CT
76642003
UMLS CUI
C0015519
Fully Specified Name
Factor X deficiency (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
21
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.