725052002: Fetal cystic fibrosis (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Fetal cystic fibrosis
• \Fetal finding\Fetal disorder\Fetus with hereditary disease\Fetal cystic fibrosis
• \Respiratory finding\Respiratory disease\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Fetal cystic fibrosis
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Inherited mucociliary clearance defect\Cystic fibrosis\Fetal cystic fibrosis
• \Disease\Genetic disease\Hereditary disease\Fetus with hereditary disease\Fetal cystic fibrosis
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Cystic fibrosis\Fetal cystic fibrosis
• \Disease\Disorder of fetus or newborn\Fetal disorder\Fetus with hereditary disease\Fetal cystic fibrosis
• \Disease\Disorder of body system\Hereditary disorder by system\Inherited mucociliary clearance defect\Cystic fibrosis\Fetal cystic fibrosis
• \Disease\Disorder of body system\Respiratory disease\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Fetal cystic fibrosis

Status: current, Defined. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3437590014	Fetal cystic fibrosis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3437591013	Fetal cystic fibrosis	en	Synonym	Active	Case insensitive	SNOMED CT core
3437592018	Foetal cystic fibrosis	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Respiratory finding reference set

Problem/Diagnosis reference set

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