700211007: Ulnar mammary syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Ulnar mammary syndrome
• \Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 12\Ulnar mammary syndrome
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 12\Ulnar mammary syndrome

Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2989585014	Ulnar mammary syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
2989606017	Ulnar mammary syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2989640017	Ulnar-mammary syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
2989657018	Schinzel syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
2989692014	An extremely rare inherited disorder characterized by malformations of the ulnar ray, hypoplasia and dysfunction of the axillary apocrine and mammary glands, endocrine dysfunction, dental anomalies, and occasional visceral malformations.	en	Definition	Active	Case sensitive	SNOMED CT core
3776280014	An extremely rare inherited disorder characterised by malformations of the ulnar ray, hypoplasia and dysfunction of the axillary apocrine and mammary glands, endocrine dysfunction, dental anomalies, and occasional visceral malformations.	en	Definition	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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