763532008: Familial nasal acilia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Respiratory finding\Respiratory disease\Familial nasal acilia
• \Disease\Disorder of body system\Respiratory disease\Familial nasal acilia
• \Disease\Familial disease\Familial nasal acilia
• \Disease\Congenital disease\Familial nasal acilia

Status: current, Primitive. 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	Case insensitive	SNOMED CT core
3642765014	Familial nasal acilia	en	Synonym	Active	Case insensitive	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	Case sensitive	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	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Respiratory finding reference set

Problem/Diagnosis reference set

Back to Start