233666007: Young's syndrome (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Inherited mucociliary clearance defect\Immotile cilia syndrome\Young's syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Immotile cilia syndrome\Young's syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Immotile cilia syndrome\Young's syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Inherited mucociliary clearance defect\Immotile cilia syndrome\Young's syndrome
\Disease\Disorder of body system\Disorder of respiratory system (disorder)\Congenital malformation of the respiratory system (disorder)\Immotile cilia syndrome\Young's syndrome
\Disease\Disorder of body system\Disorder of respiratory system (disorder)\Mucociliary clearance defect\Inherited mucociliary clearance defect\Immotile cilia syndrome\Young's syndrome
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital malformation syndrome (disorder)\Malformation sequence\Immotile cilia syndrome\Young's syndrome
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital malformation of the respiratory system (disorder)\Immotile cilia syndrome\Young's syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Immotile cilia syndrome\Young's syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome (disorder)\Malformation sequence\Immotile cilia syndrome\Young's syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital malformation of the respiratory system (disorder)\Immotile cilia syndrome\Young's syndrome

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Young's syndrome	Is a	Immotile cilia syndrome	true	Inferred relationship	Some
Young's syndrome	Occurrence	Congenital	false	Inferred relationship	Some
Young's syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Some
Young's syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Young's syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Some	1
Young's syndrome	Associated morphology	defect	false	Inferred relationship	Some	2
Young's syndrome	Finding site	Respiratory tract structure	false	Inferred relationship	Some	2
Young's syndrome	Has interpretation	Impaired	true	Inferred relationship	Some	3
Young's syndrome	Interprets	Mucociliary clearance	true	Inferred relationship	Some	3
Young's syndrome	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1
Young's syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Young's syndrome	Finding site	Respiratory tract structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
350131018	Young's syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
350132013	Azoospermia, obstructive and chronic sinopulmonary infections	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
350133015	Sinusitis-infertility syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
350134014	Barry-Perkins-Young syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
621881011	Young's syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2838642016	Young syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
885941000172117	syndrome d'azoospermie, infections pulmonaires, sinusite	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
897681000172113	syndrome de Young	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
920471000172112	azoöspermie, sinopulmonale infecties	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
987931000172112	syndroom van Young	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
1015061000172116	Young-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)