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763532008: Familial nasal acilia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3642764013 Familial nasal acilia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3642765014 Familial nasal acilia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404095016 Familial nasal acilia is a rare genetic otorhinolaryngologic disease characterized by respiratory morbidity due to lack of cilia on the respiratory tract epithelial cells. The disease manifests from birth with respiratory distress, neonatal pneumonia, dyspnea, lobar atelectasis and bronchiectasis. Recurrent infections of the upper and lower respiratory tract, chronic humid coughing, and chronic sinusitis, otitis and rhinitis are typical lifelong presenting conditions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404096015 Familial nasal acilia is a rare genetic otorhinolaryngologic disease characterised by respiratory morbidity due to lack of cilia on the respiratory tract epithelial cells. The disease manifests from birth with respiratory distress, neonatal pneumonia, dyspnoea, lobar atelectasis and bronchiectasis. Recurrent infections of the upper and lower respiratory tract, chronic humid coughing, and chronic sinusitis, otitis and rhinitis are typical lifelong presenting conditions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3642764013 Familial nasal acilia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3642765014 Familial nasal acilia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3642766010 A rare genetic otorhinolaryngologic disease characterised by respiratory morbidity due to lack of cilia on the respiratory tract epithelial cells. The disease manifests from birth with respiratory distress, neonatal pneumonia, dyspnoea, lobar atelectasis and bronchiectasis. Recurrent infections of the upper and lower respiratory tract, chronic humid coughing, and chronic sinusitis, otitis and rhinitis are typical lifelong presenting conditions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3642767018 A rare genetic otorhinolaryngologic disease characterized by respiratory morbidity due to lack of cilia on the respiratory tract epithelial cells. The disease manifests from birth with respiratory distress, neonatal pneumonia, dyspnea, lobar atelectasis and bronchiectasis. Recurrent infections of the upper and lower respiratory tract, chronic humid coughing, and chronic sinusitis, otitis and rhinitis are typical lifelong presenting conditions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404095016 Familial nasal acilia is a rare genetic otorhinolaryngologic disease characterized by respiratory morbidity due to lack of cilia on the respiratory tract epithelial cells. The disease manifests from birth with respiratory distress, neonatal pneumonia, dyspnea, lobar atelectasis and bronchiectasis. Recurrent infections of the upper and lower respiratory tract, chronic humid coughing, and chronic sinusitis, otitis and rhinitis are typical lifelong presenting conditions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404096015 Familial nasal acilia is a rare genetic otorhinolaryngologic disease characterised by respiratory morbidity due to lack of cilia on the respiratory tract epithelial cells. The disease manifests from birth with respiratory distress, neonatal pneumonia, dyspnoea, lobar atelectasis and bronchiectasis. Recurrent infections of the upper and lower respiratory tract, chronic humid coughing, and chronic sinusitis, otitis and rhinitis are typical lifelong presenting conditions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3441891001000111 Syndrom der fehlenden Nasenzilien, familiäre Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
943331000172111 absence familiale de cils nasaux fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
943331000172111 absence familiale de cils nasaux fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3441891001000111 Syndrom der fehlenden Nasenzilien, familiäre Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial nasal acilia Is a Disorder of respiratory system false Inferred relationship Existential restriction modifier (core metadata concept)
Familial nasal acilia Is a Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept)
Familial nasal acilia Is a Familial disease true Inferred relationship Existential restriction modifier (core metadata concept)
Familial nasal acilia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial nasal acilia Finding site Structure of respiratory epithelium (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial nasal acilia Is a Respiratory condition of fetus OR newborn true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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