WNT4 Mullerian aplasia and ovarian dysfunction

disorder

SNOMED 699275001CUI C3697628

Overview

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

Related Conditions

Hereditary disorder of endocrine system(parent)

Mullerian aplasia(parent)

Disorder of endocrine ovary(parent)

Reproductive system hereditary disorder(parent)

Quick Facts

SNOMED CT: 699275001
UMLS CUI: C3697628
Fully Specified Name: WNT4 Müllerian aplasia and ovarian dysfunction (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.