205824006: Noonan's syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary neoplastic syndrome\Noonan's syndrome
• \Developmental hereditary disorder\Noonan's syndrome
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Noonan's syndrome
• \Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome, moderate short stature, facial\Noonan's syndrome
• \Developmental disorder\Developmental hereditary disorder\Noonan's syndrome
• \Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome, moderate short stature, facial\Noonan's syndrome

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2475674013	Noonan-Ehmke syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
2475675014	Turner-like syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
2475676010	Noonan syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
315625018	Noonan's syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
591246012	Noonan's syndrome (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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