253828000: Mullerian aplasia (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Developmental hereditary disorder\Mullerian aplasia
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Mullerian aplasia
• \Disorder of embryonic structure\Mullerian aplasia
• \Congenital disease\Congenital anomaly\Mullerian aplasia
• \Developmental disorder\Developmental hereditary disorder\Mullerian aplasia
• \Developmental disorder\Congenital anomaly\Mullerian aplasia

Status: current, Defined. Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
377915012	Mullerian aplasia	en	Synonym	Active	Case sensitive	SNOMED CT core
3786955011	Müllerian duct failure	en	Synonym	Active	Case sensitive	SNOMED CT core
3792846014	Aplasia of Müllerian ducts	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
644635015	Mullerian aplasia (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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