255399007: Congenital (qualifier value)

SNOMED CT Concept\Qualifier value\...

\Precondition value (qualifier value)\Periods of life\Congenital

\Special atomic mapping values\Special disorder atoms\Temporal periods\Periods of life\Congenital

\Descriptor (qualifier value)\Time patterns\Temporal periods\Periods of life\Congenital

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
Congenital	Is a	Periods of life	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
BRESEK syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypergonadotropic hypogonadism with cataract syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Hypergonadotropic hypogonadism with cataract syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Acrofrontofacionasal dysostosis type 2	Occurrence	False	Congenital	Inferred relationship	Some	5
Acrofrontofacionasal dysostosis type 2	Occurrence	False	Congenital	Inferred relationship	Some	6
Acrofrontofacionasal dysostosis type 2	Occurrence	False	Congenital	Inferred relationship	Some	7
Acrofrontofacionasal dysostosis type 2	Occurrence	False	Congenital	Inferred relationship	Some	8
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Joubert syndrome with congenital hepatic fibrosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Joubert syndrome with congenital hepatic fibrosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Joubert syndrome with oculorenal defect (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Joubert syndrome with orofaciodigital defect (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	5
Joubert syndrome with orofaciodigital defect (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	6
Joubert syndrome with orofaciodigital defect (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Joubert syndrome with orofaciodigital defect (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	8
Joubert syndrome with orofaciodigital defect (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	9
Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Limb mammary syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Limb mammary syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Limb mammary syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Limb mammary syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Lipodystrophy, intellectual disability, deafness syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Lipodystrophy, intellectual disability, deafness syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Lowry MacLean syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Lowry MacLean syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Lowry MacLean syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Lung agenesis with heart defect and thumb anomaly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Lung agenesis with heart defect and thumb anomaly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Lung agenesis with heart defect and thumb anomaly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Lymphedema, atrial septal defect, facial changes syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Lymphedema, atrial septal defect, facial changes syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Lymphedema, atrial septal defect, facial changes syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Lymphedema and cerebral arteriovenous anomaly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Lymphedema and cerebral arteriovenous anomaly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	8
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	9
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	10
Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Multiple mitochondrial dysfunctions syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Thoracic insufficiency syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Thoracic insufficiency syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Adult polyglucosan body disease (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Component of oligomeric golgi complex 5 congenital disorder of glycosylation (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Klippel Trenaunay syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Joubert syndrome with oculorenal defect (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Congenital cerebral ventriculomegaly (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
megalencefalisyndrom med kapillär missbildning	Occurrence	False	Congenital	Inferred relationship	Some	1
Megalencephalic leukoencephalopathy with subcortical cysts	Occurrence	True	Congenital	Inferred relationship	Some	1
Mesomelic dysplasia with cleft palate and camptodactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Multiple epiphyseal dysplasia type 4 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Multiple epiphyseal dysplasia type 1 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Multiple epiphyseal dysplasia type 5 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Brachydactyly type A1 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Unilateral polymicrogyria (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Blepharocheilodontic syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Blepharocheilodontic syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Multiple epiphyseal dysplasia Al-Gazali type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Multiple epiphyseal dysplasia Beighton type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Eiken syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Hip dysplasia Beukes type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Long gap atresia of esophagus (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital diverticulitis of small intestine (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital diverticulosis of small intestine (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital diverticulosis of small intestine (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Hypertelorism with microtia and facial clefting syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Hypertelorism with microtia and facial clefting syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Hypertelorism with microtia and facial clefting syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Hypertelorism with microtia and facial clefting syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Intellectual disability, balding, patella luxation, acromicria syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Intellectual disability, balding, patella luxation, acromicria syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Intellectual disability, balding, patella luxation, acromicria syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
syndrom med intellektuell funktionsnedsättning, katarakt och kyfos	Occurrence	False	Congenital	Inferred relationship	Some	3
syndrom med intellektuell funktionsnedsättning, katarakt och kyfos	Occurrence	False	Congenital	Inferred relationship	Some	4
Agenesis of internal carotid artery (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Isotretinoin embryopathy-like syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Isotretinoin embryopathy-like syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Isotretinoin embryopathy-like syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Isotretinoin embryopathy-like syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Kapur Toriello syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Kapur Toriello syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Karsch Neugebauer syndrome	Occurrence	True	Congenital	Inferred relationship	Some	5
Karsch Neugebauer syndrome	Occurrence	False	Congenital	Inferred relationship	Some	6
Karsch Neugebauer syndrome	Occurrence	False	Congenital	Inferred relationship	Some	7
Karsch Neugebauer syndrome	Occurrence	False	Congenital	Inferred relationship	Some	8
Karsch Neugebauer syndrome	Occurrence	False	Congenital	Inferred relationship	Some	9
Macrocephaly, short stature, paraplegia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7

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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
135131000052119	medfödd	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)