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
Overgrowth, macrocephaly, facial dysmorphism syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypomandibular faciocranial dysostosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Lumbar spina bifida with hydrocephalus	Occurrence	True	Congenital	Inferred relationship	Some	4
Dysspondyloenchondromatosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Anomalous pulmonary venous drainage to hepatic veins	Occurrence	True	Congenital	Inferred relationship	Some	2
Transient mitral regurgitation of newborn	Occurrence	False	Congenital	Inferred relationship	Some	1
Juvenile idiopathic generalized osteoporosis	Occurrence	False	Congenital	Inferred relationship	Some	1
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Persistent thyroglossal duct	Occurrence	True	Congenital	Inferred relationship	Some	1
Nager syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Bilateral hypoplasia of tibia and postaxial polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Female pseudohermaphroditism	Occurrence	False	Congenital	Inferred relationship	Some	2
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Encephalocele of orbit	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital pontocerebellar hypoplasia type 6 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Generalized macrodontia	Occurrence	False	Congenital	Inferred relationship	Some	1
Beals auriculo-osteodysplasia syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Omphalomesenteric duct cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Spondyloepimetaphyseal dysplasia Irapa type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Muscle-eye-brain disease, congenital muscular dystrophy	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete ossification of centrum of sacral vertebra	Occurrence	True	Congenital	Inferred relationship	Some	1
Ossification anomaly with psychomotor developmental delay syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Ossification anomaly with psychomotor developmental delay syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Persistent aortic arch convolutions	Occurrence	True	Congenital	Inferred relationship	Some	1
Odontoma dysphagia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Basan syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Camptodactyly syndrome Guadalajara type 1 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Camptodactyly syndrome Guadalajara type 1 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Camptodactyly syndrome Guadalajara type 1 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
cervikalt spinalt hydromeningocele	Occurrence	False	Congenital	Inferred relationship	Some	3
cervikalt spinalt hydromeningocele	Occurrence	False	Congenital	Inferred relationship	Some	1
Multinodular goiter, cystic kidney, polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Multinodular goiter, cystic kidney, polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Multinodular goiter, cystic kidney, polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Interrupted aortic arch between left common carotid and brachiocephalic artery	Occurrence	True	Congenital	Inferred relationship	Some	1
Abnormal communication between pericardial sac and peritoneal cavity	Occurrence	True	Congenital	Inferred relationship	Some	1
Czech dysplasia metatarsal type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Multirooted tooth with divergent roots	Occurrence	False	Congenital	Inferred relationship	Some	1
Absent tibia, polydactyly, arachnoid cyst syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Absent tibia, polydactyly, arachnoid cyst syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Pseudo-Hurler polydystrophy	Occurrence	True	Congenital	Inferred relationship	Some	1
Rachischisis with hydrocephalus	Occurrence	True	Congenital	Inferred relationship	Some	4
Rachischisis with hydrocephalus	Occurrence	True	Congenital	Inferred relationship	Some	1
Rachischisis with hydrocephalus	Occurrence	True	Congenital	Inferred relationship	Some	3
BSG syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
BSG syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Capillary-venous-lymphatic malformation (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Capillary-venous-lymphatic malformation (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
övertalig kusp	Occurrence	False	Congenital	Inferred relationship	Some	1
Aplasia of muscle	Occurrence	True	Congenital	Inferred relationship	Some	1
Right ventricular outflow tract obstruction due to common atrioventricular valve (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Ectodermal dysplasia, syndactyly and pili torti	Occurrence	True	Congenital	Inferred relationship	Some	1
Anodontia of permanent dentition	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete ossification of tibia	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypogonadism with prune belly syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Spondyloepimetaphyseal disorder	Occurrence	True	Congenital	Inferred relationship	Some	1
Kallman syndrome with heart disease (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Spina bifida	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital horizontal mandibular hypoplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Muscular ventricular septal defect in central trabecular septum	Occurrence	True	Congenital	Inferred relationship	Some	1
Cerebro-facio-thoracic dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cerebro-facio-thoracic dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Polyorchism	Occurrence	True	Congenital	Inferred relationship	Some	1
Spondyloenchondrodysplasia with immune dysregulation	Occurrence	True	Congenital	Inferred relationship	Some	1
Double kidney	Occurrence	True	Congenital	Inferred relationship	Some	1
Progressive junctional epidermolysis bullosa (neurotrophic)	Occurrence	True	Congenital	Inferred relationship	Some	1
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Multiple neurofibromas in neurofibromatosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Multiple neurofibromas in neurofibromatosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Diffuse hypoplasia of right ventricle	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Amelogenesis imperfecta, pigmented hypomaturation type	Occurrence	True	Congenital	Inferred relationship	Some	1
Low assimilation pelvis	Occurrence	True	Congenital	Inferred relationship	Some	1
Johnson neuroectodermal syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Tibial aplasia and ectrodactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrial septal defect, atrioventricular conduction defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Enamel-renal syndrome	Occurrence	False	Congenital	Inferred relationship	Some	1
Rud's syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
dysplasi karakteriserad av böjning av skelettben	Occurrence	False	Congenital	Inferred relationship	Some	1
Fibrochondrogenesis	Occurrence	True	Congenital	Inferred relationship	Some	1
Ectopic glial tissue	Occurrence	True	Congenital	Inferred relationship	Some	1
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Peutz-Jeghers syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
Hypodontia and nail dysgenesis	Occurrence	True	Congenital	Inferred relationship	Some	3
parodontit samtidigt med Ehlers-Danlos syndrom typ 4	Occurrence	False	Congenital	Inferred relationship	Some	1
parodontit samtidigt med Ehlers-Danlos syndrom typ 4	Occurrence	False	Congenital	Inferred relationship	Some	3
Nasopalpebral lipoma coloboma syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
cervikala, vaginala och externa anomalier i kvinnliga könsorgan	Occurrence	True	Congenital	Inferred relationship	Some	1
Myeloschisis	Occurrence	True	Congenital	Inferred relationship	Some	1
Frontofacionasal dysplasia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Ulna fibula ray defect and brachydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Ulna fibula ray defect and brachydactyly syndrome (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)