Acquired protein C deficiency

disorder

SNOMED 1217410004CUI C2674322

Overview

Acquired protein C deficiency 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.

Abnormality of the nervous system

HP:0000707

Blood clot in artery of lung

HP:0002204

Cerebral thrombosis

HP:0005305

Deep venous thrombosis

HP:0002625

Eye disease

HP:0000478

Hypercoagulability

HP:0100724

Protein C deficiency

HP:0005543

Superficial thrombophlebitis

HP:0002638

Warfarin-induced skin necrosis

HP:0001038

Related Conditions

Acquired coagulation disorder(parent)

Acquired thrombophilia(parent)

Protein C deficiency disease(parent)

Quick Facts

SNOMED CT: 1217410004
UMLS CUI: C2674322
Fully Specified Name: Acquired protein C deficiency (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.