von Willebrand disease type 2N

disorder

SNOMED 359732009CUI C1282975

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.

Bruising susceptibility

HP:0000978

Frequent nosebleeds

HP:0000421

Hypermenorrhea

HP:0000132

Thrombocytopenia

HP:0001873

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

von Willebrand disease type 2(parent)

Quick Facts

SNOMED CT: 359732009
UMLS CUI: C1282975
Fully Specified Name: Hereditary von Willebrand disease type 2N (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 4

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.