255399007: congenitaal (kwalificatiewaarde)

SNOMED CT Concept\Qualifier value\...

\Precondition value (qualifier value)\Periods of life\Fetal and/or neonatal period\Congenital

\Special atomic mapping values\Special disorder atoms\Temporal periods\Periods of life\Fetal and/or neonatal period\Congenital

\Descriptor (qualifier value)\Time patterns\Temporal periods\Periods of life\Fetal and/or neonatal period\Congenital

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

380598010 Congenital en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

380599019 Congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

646433016 Congenital (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3440841000146116 congenitaal nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

3440851000146118 congenitaal (kwalificatiewaarde) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

3440861000146115 aangeboren nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital	Is a	Periods of life	false	Inferred relationship	Some
Congenital	Is a	Fetal and/or neonatal period	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Male microcephalus, hypergonadotropic hypogonadism, short stature syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Female albinism with deafness syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Female albinism with deafness syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Male albinism with deafness syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Male albinism with deafness syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Male albinism with deafness syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
congenitale spondylolyse (aandoening)	Occurrence	False	Congenital	Inferred relationship	Some	1
Complete transposition of great vessels with ventricular septal defect (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Telomere biology disorder (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Longitudinal deficiency of upper arm (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1

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Reference Sets

Dutch pathology simple reference set (foundation metadata concept)