1296527009: Cystic fibrosis due to heterozygous deltaF508 mutation (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Finding of respiratory function (finding)\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis due to heterozygous deltaF508 mutation
• \Respiratory finding\Finding of respiration\Finding of respiratory function (finding)\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis due to heterozygous deltaF508 mutation
• \Respiratory finding\Disorder of respiratory system\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis due to heterozygous deltaF508 mutation
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis due to heterozygous deltaF508 mutation
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Cystic fibrosis\Cystic fibrosis due to heterozygous deltaF508 mutation
• \Disease\Disorder of body system\Hereditary disorder by system (disorder)\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis due to heterozygous deltaF508 mutation
• \Disease\Disorder of body system\Disorder of respiratory system\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis due to heterozygous deltaF508 mutation

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Dec 2023. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5285688016	Cystic fibrosis due to heterozygous deltaF508 mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5285689012	DeltaF508 heterozygous mucoviscidosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5285690015	Cystic fibrosis due to heterozygous deltaF508 mutation (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5285691016	DeltaF508 heterozygous cystic fibrosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5285688016	Cystic fibrosis due to heterozygous deltaF508 mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5285689012	DeltaF508 heterozygous mucoviscidosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5285690015	Cystic fibrosis due to heterozygous deltaF508 mutation (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5285691016	DeltaF508 heterozygous cystic fibrosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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