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63533009: Mucociliary clearance, function (observable entity)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
105598012 Mucociliary clearance en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1204077019 Mucociliary clearance, function (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2671421012 Mucociliary clearance, function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1797301000172112 clairance mucociliaire, fonction fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
1797311000172110 clairance mucociliaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
1444501000172113 mucociliaire clearance nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
1444511000172111 mucociliaire klaring nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mucociliary clearance Is a Respiratory function true Inferred relationship Some
Mucociliary clearance Is a Physiological functions and activities false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Kartagener syndrome Interprets True Mucociliary clearance Inferred relationship Some 5
Cystic fibrosis without meconium ileus Interprets True Mucociliary clearance Inferred relationship Some 1
Cystic fibrosis with meconium ileus Interprets True Mucociliary clearance Inferred relationship Some 3
Immotile cilia syndrome Interprets True Mucociliary clearance Inferred relationship Some 3
Cystic fibrosis of the lung Interprets True Mucociliary clearance Inferred relationship Some 2
Cystic fibrosis Interprets True Mucociliary clearance Inferred relationship Some 1
Mucociliary clearance defect Interprets True Mucociliary clearance Inferred relationship Some 1
Inherited mucociliary clearance defect Interprets True Mucociliary clearance Inferred relationship Some 1
Primary ciliary dyskinesia due to transposition of ciliary microtubules Interprets True Mucociliary clearance Inferred relationship Some 3
Immotile cilia syndrome due to defective radial spokes Interprets True Mucociliary clearance Inferred relationship Some 3
Immotile cilia syndrome due to excessively long cilia Interprets True Mucociliary clearance Inferred relationship Some 1
Young's syndrome Interprets True Mucociliary clearance Inferred relationship Some 3
Rutland ciliary disorientation syndrome Interprets True Mucociliary clearance Inferred relationship Some 3
Acquired mucociliary clearance defect Interprets True Mucociliary clearance Inferred relationship Some 1
Secondary ciliary dyskinesia Interprets True Mucociliary clearance Inferred relationship Some 1
Transient mucociliary clearance defect Interprets True Mucociliary clearance Inferred relationship Some 2
Cystic fibrosis of pancreas Interprets True Mucociliary clearance Inferred relationship Some 2
Diabetes mellitus associated with cystic fibrosis Interprets True Mucociliary clearance Inferred relationship Some 2
Exocrine pancreatic manifestation co-occurrent and due to cystic fibrosis (disorder) Interprets True Mucociliary clearance Inferred relationship Some 2
Follicular hamartoma with alopecia and cystic fibrosis syndrome (disorder) Interprets True Mucociliary clearance Inferred relationship Some 1
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) Interprets True Mucociliary clearance Inferred relationship Some 4
Fetal cystic fibrosis (disorder) Interprets True Mucociliary clearance Inferred relationship Some 2
Cystic fibrosis with intestinal manifestations Interprets False Mucociliary clearance Inferred relationship Some 1
Cystic fibrosis with gastritis and megaloblastic anemia syndrome (disorder) Interprets True Mucociliary clearance Inferred relationship Some 2
Classical cystic fibrosis (disorder) Interprets True Mucociliary clearance Inferred relationship Some 2
Atypical cystic fibrosis (disorder) Interprets True Mucociliary clearance Inferred relationship Some 2
Subclinical cystic fibrosis Interprets True Mucociliary clearance Inferred relationship Some 2

This concept is not in any reference sets

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