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
Ulna fibula ray defect and brachydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Ulna fibula ray defect and brachydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Multiple anterior segment anomalies	Occurrence	True	Congenital	Inferred relationship	Some	1
Atelosteogenesis type 2	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrioventricular septal defect - ventricular component	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital prolapse of urethra	Occurrence	True	Congenital	Inferred relationship	Some	1
Bertolotti's syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital pontocerebellar hypoplasia type 5 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypospadias and epispadias	Occurrence	True	Congenital	Inferred relationship	Some	1
Laryngo-onycho-cutaneous syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Laryngo-onycho-cutaneous syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Dominant dystrophic epidermolysis bullosa, albopapular type	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete ossification of centrum of thoracic vertebra	Occurrence	True	Congenital	Inferred relationship	Some	1
medfödd muskeldystrofi	Occurrence	False	Congenital	Inferred relationship	Some	1
Microphthalmia with linear skin defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Greither type of ectodermal dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Isolation of left common carotid artery (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Dermatofibrosis lenticularis disseminata	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital hyperplasia of sebaceous glands of lip	Occurrence	True	Congenital	Inferred relationship	Some	1
Cortical blindness, intellectual disability, polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Cortical blindness, intellectual disability, polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cortical blindness, intellectual disability, polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Cloverleaf skull with multiple congenital anomalies syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cloverleaf skull with multiple congenital anomalies syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Cloverleaf skull with multiple congenital anomalies syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Cloverleaf skull with multiple congenital anomalies syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	5
Cloverleaf skull with multiple congenital anomalies syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Erythrodermic lamellar ichthyosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Deafness, vitiligo, achalasia syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Deafness, vitiligo, achalasia syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Myelocele with hydrocephalus	Occurrence	True	Congenital	Inferred relationship	Some	5
Myelocele with hydrocephalus	Occurrence	True	Congenital	Inferred relationship	Some	2
osteokondrodysplasi	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital portal-systemic shunt	Occurrence	True	Congenital	Inferred relationship	Some	1
Obstruction of right ventricular outflow tract due to aortico-left ventricular tunnel (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital hypoplasia of cerebrum	Occurrence	True	Congenital	Inferred relationship	Some	1
Constricting band of extremity (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Superior to inferior ventricular relationship (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Van den Ende-Gupta syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Van den Ende-Gupta syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Talon cusp	Occurrence	False	Congenital	Inferred relationship	Some	1
Osseous syndactyly of toes first web space	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete ossification of tympanic anulus	Occurrence	True	Congenital	Inferred relationship	Some	1
Ectodermal dysplasia trichoodontoonychial type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Ectodermal dysplasia trichoodontoonychial type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Holoanencephaly (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Sacral hemivertebra	Occurrence	True	Congenital	Inferred relationship	Some	1
Bipartite ossification of sternebra	Occurrence	True	Congenital	Inferred relationship	Some	1
Goniodysgenesis with intellectual disability and short stature syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Vascular ring with left aortic arch and right patent arterial duct (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Vascular ring with left aortic arch and right arterial duct arising from retroesophageal aortic diverticulum (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Autosomal recessive ocular albinism (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Accessory ossification center	Occurrence	True	Congenital	Inferred relationship	Some	1
Vascular ring with left aortic arch to right descending aorta and right patent arterial duct (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Thoracic spina bifida with hydrocephalus - open	Occurrence	True	Congenital	Inferred relationship	Some	3
Vascular ring with left aortic arch and retroesophageal right descending aorta and right arterial duct arising from aortic diverticulum and aberrant right subclavian artery (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Sacral spina bifida with hydrocephalus - open (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Infracardiac location of anomalous pulmonary venous connection with two descending veins (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Posterior lenticonus	Occurrence	True	Congenital	Inferred relationship	Some	1
metafyseal kondrodysplasi, McKusick-typ med associerad immunbrist	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenital hernia of foramen of Morgagni	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital hernia of foramen of Morgagni	Occurrence	True	Congenital	Inferred relationship	Some	2
German syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Diaphragmatic defect, limb deficiency, skull defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Diaphragmatic defect, limb deficiency, skull defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Retinal detachment and occipital encephalocele	Occurrence	True	Congenital	Inferred relationship	Some	4
Localised macrodontia	Occurrence	False	Congenital	Inferred relationship	Some	1
Infracardiac location of anomalous pulmonary venous connection to hepatic vein (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Ocular albinism	Occurrence	True	Congenital	Inferred relationship	Some	1
Hereditary hypotrichosis with recurrent skin vesicles syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Pachyonychia congenita type III of Schafer-Brunauer (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
okulär albinism - lentiginos - dövhetssyndrom	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Craniosynostosis Boston type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Congenital venous malformation of skin (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Ocular albinism, type I	Occurrence	True	Congenital	Inferred relationship	Some	1
Fetal genitourinary abnormality (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Craniosynostosis Philadelphia type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Vascular ring with left aortic arch to right descending aorta and right arterial ligament (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Microcephalus cardiomyopathy syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Albinism co-occurrent with hematologic disorder (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Aland eye disease and ocular albinism	Occurrence	True	Congenital	Inferred relationship	Some	1
Raised birthmark	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital cataract, nephropathy, encephalopathy syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Vascular ring with left aortic arch and right arterial duct ligament arising from retroesophageal aortic diverticulum with aberrant right subclavian artery (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Lumbar spina bifida with hydrocephalus - open	Occurrence	True	Congenital	Inferred relationship	Some	5
Ocular albinism with late-onset sensorineural deafness (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Pachyonychia congenita type II of Jackson-Lawler (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deafness, enamel hypoplasia, nail defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Familial digital arthropathy and brachydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Nasofrontal encephalocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Nasofrontal encephalocele	Occurrence	False	Congenital	Inferred relationship	Some	3
hydrencefalomeningocele	Occurrence	False	Congenital	Inferred relationship	Some	1
hydrencefalomeningocele	Occurrence	False	Congenital	Inferred relationship	Some	2
Nasopharyngeal encephalocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Nasopharyngeal encephalocele	Occurrence	False	Congenital	Inferred relationship	Some	3
Autosomal dominant palmoplantar keratoderma and congenital alopecia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Vascular ring with left aortic arch and right arterial duct arising from aberrant retroesophageal brachiocephalic artery (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Vascular ring with left aortic arch and retrotracheal right patent arterial duct (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1

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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)