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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
61191000077116 clairance mucociliaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mucociliary clearance Is a Any function involved in the exchange of oxygen and carbon dioxide between the atmosphere and the cells of the body true Inferred relationship Some
Mucociliary clearance Is a fonctions et activités physiologiques 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
diabète sucré concomitant et dû à la mucoviscidose Interprets False 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 - retinitis pigmentosa is an X-linked ciliary dysfunction of both respiratory epithelium and photoreceptors of the retina leading to ocular disorders (mild night blindness, constriction of the visual field, and scotopic and photopic ERG responses reduced to 30-60%) associated with primary ciliary dyskinesia manifestations (chronic bronchorrhea with bronchiectasis and chronic sinusitis) and sensorineural hearing loss. 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
A rare genetic disease characterized by cystic fibrosis, gastritis associated with Helicobacter pylori, folate deficiency megaloblastic anemia, and intellectual disability. There have been no further descriptions in the literature since 1991. 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
Cystic fibrosis due to heterozygous deltaF508 mutation Interprets True Mucociliary clearance Inferred relationship Some 1
Cystic fibrosis due to homozygous deltaF508 mutation Interprets True Mucociliary clearance Inferred relationship Some 1
Diabetes mellitus due to cystic fibrosis (disorder) Interprets True Mucociliary clearance Inferred relationship Some 1

This concept is not in any reference sets

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