233661002: Inherited mucociliary clearance defect (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Finding of respiratory function (finding)\Mucociliary clearance defect\Inherited mucociliary clearance defect

\Respiratory finding\Finding of respiration\Finding of respiratory function (finding)\Mucociliary clearance defect\Inherited mucociliary clearance defect
\Respiratory finding\Disorder of respiratory system\Mucociliary clearance defect\Inherited mucociliary clearance defect

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Inherited mucociliary clearance defect
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Inherited mucociliary clearance defect
\Disease\Disorder of body system\Disorder of respiratory system\Mucociliary clearance defect\Inherited mucociliary clearance defect

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

350123011 Inherited mucociliary clearance defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

621875015 Inherited mucociliary clearance defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5144466017 Inherited impaired mucociliary clearance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5144467014 Inherited defective mucociliary clearance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

350123011 Inherited mucociliary clearance defect en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

350123011 Inherited mucociliary clearance defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

621875015 Inherited mucociliary clearance defect (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

621875015 Inherited mucociliary clearance defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5144466017 Inherited impaired mucociliary clearance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5144467014 Inherited defective mucociliary clearance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4987381000241111 défaut de clairance mucociliaire héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4987381000241111 défaut de clairance mucociliaire héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Inherited mucociliary clearance defect	Is a	Mucociliary clearance defect	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Inherited mucociliary clearance defect	Has interpretation	Impaired (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Inherited mucociliary clearance defect	Interprets	Mucociliary clearance	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Inherited mucociliary clearance defect	Associated morphology	Defect	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Inherited mucociliary clearance defect	Finding site	Respiratory tract structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Inherited mucociliary clearance defect	Is a	Hereditary disorder by system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cystic fibrosis	Is a	True	Inherited mucociliary clearance defect	Inferred relationship	Existential restriction modifier (core metadata concept)
Immotile cilia syndrome	Is a	True	Inherited mucociliary clearance defect	Inferred relationship	Existential restriction modifier (core metadata concept)
Immotile cilia syndrome due to excessively long cilia	Is a	True	Inherited mucociliary clearance defect	Inferred relationship	Existential restriction modifier (core metadata concept)
Cystic fibrosis of pancreas	Is a	False	Inherited mucociliary clearance defect	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder)	Is a	True	Inherited mucociliary clearance defect	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets