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Mullerian aplasia

disorder
SNOMED 253828000CUI C0431637

Overview

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

Related Conditions

WNT4 Mullerian aplasia and ovarian dysfunction(child)
Disorder of embryonic structure(parent)
Congenital malformation(parent)
Autosomal dominant hereditary disorder(parent)
Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT
253828000
UMLS CUI
C0431637
Fully Specified Name
Mullerian aplasia (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.