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
Crisponi syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Crisponi syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Crisponi syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital pulmonary arteriovenous aneurysm	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital leukonychia	Occurrence	True	Congenital	Inferred relationship	Some	1
Aortic left ventricular tunnel with right coronary artery from tunnel (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Acromelanosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Diaphanospondylodysostosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Atrioventricular septal defect with ventricular component under superior bridging leaflet with chords to papillary muscle on right ventricular side septum (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Lethal recessive chondrodysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Roberts-SC phocomelia syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Anterior imbrication of teeth	Occurrence	False	Congenital	Inferred relationship	Some	1
Right superior vena cava connecting to left atrium and right atrium (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Ectodermal dysplasia with natal teeth Turnpenny type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Thoracic spina bifida with hydrocephalus - closed	Occurrence	True	Congenital	Inferred relationship	Some	1
Hyperplastic tooth follicle	Occurrence	False	Congenital	Inferred relationship	Some	1
Hyperplastic tooth follicle	Occurrence	False	Congenital	Inferred relationship	Some	2
Disorganized development of cartilaginous and fibrous components of the skeleton	Occurrence	True	Congenital	Inferred relationship	Some	1
Uterus bicornuatus vetularum	Occurrence	True	Congenital	Inferred relationship	Some	1
Kniest-Sticklers dysplasigrupp	Occurrence	False	Congenital	Inferred relationship	Some	1
multipel medfödd ledstelhet	Occurrence	False	Congenital	Inferred relationship	Some	1
Simple syndactyly of toes of bilateral feet (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Radial polydactyly Wassel 6	Occurrence	False	Congenital	Inferred relationship	Some	1
Interrupted aortic arch between left subclavian and left common carotid artery	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital abnormality of atrioventricular valves in atrioventricular septal defect (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Septate vagina affecting pregnancy	Occurrence	True	Congenital	Inferred relationship	Some	1
polydaktyli i tumme	Occurrence	False	Congenital	Inferred relationship	Some	1
Ectodermal dysplasia-ocular malformation syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Epidermolysis bullosa simplex, Ogna type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Lingual thyroid	Occurrence	True	Congenital	Inferred relationship	Some	1
Short stature with webbed neck and congenital heart disease syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Short stature with webbed neck and congenital heart disease syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Ichthyosis, oral and digital anomalies syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Ichthyosis, oral and digital anomalies syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
neurokutan melanos	Occurrence	False	Congenital	Inferred relationship	Some	1
Isolation of left subclavian artery (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Ectopic liver (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Holoprosencephaly craniosynostosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Acrocephalosyndactyly type I	Occurrence	True	Congenital	Inferred relationship	Some	1
Acrocephalosyndactyly type I	Occurrence	True	Congenital	Inferred relationship	Some	2
Macrocephaly, obesity, mental disability, ocular abnormality syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Macrocephaly, obesity, mental disability, ocular abnormality syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Oculoosteocutaneous syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Adult fucosidosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Notomelus	Occurrence	True	Congenital	Inferred relationship	Some	1
Growth delay with hydrocephalus and lung hypoplasia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital hereditary facial paralysis with variable hearing loss syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital hereditary facial paralysis with variable hearing loss syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Contracture with ectodermal dysplasia and orofacial cleft syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Contracture with ectodermal dysplasia and orofacial cleft syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Cataract and microcornea syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Fusion of crown of teeth	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital coronary artery fistula to left atrium	Occurrence	True	Congenital	Inferred relationship	Some	1
Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Patent ductus arteriosus - delayed closure (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Leri's pleonosteosis syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Ichthyosis congenita with biliary atresia	Occurrence	True	Congenital	Inferred relationship	Some	1
Acrofacial dysostosis Catania type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Laryngeal cleft type I	Occurrence	True	Congenital	Inferred relationship	Some	1
Urachal diverticulum (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Spondylocamptodactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital corneal opacity not interfering with vision	Occurrence	True	Congenital	Inferred relationship	Some	1
Anomalous pulmonary venous drainage to right atrium	Occurrence	True	Congenital	Inferred relationship	Some	2
Radioulnar synostosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypoplasia of right ventricular inflow tract (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
syndrom med hypospadi, hypertelorism, kolobom och dövhet	Occurrence	False	Congenital	Inferred relationship	Some	1
syndrom med hypospadi, hypertelorism, kolobom och dövhet	Occurrence	False	Congenital	Inferred relationship	Some	3
syndrom med hypospadi, hypertelorism, kolobom och dövhet	Occurrence	False	Congenital	Inferred relationship	Some	2
Absent ductus venosus with direct connection of umbilical vein to renal vein (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Absent ductus venosus with direct connection of umbilical vein to renal vein (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Absent ductus venosus with direct connection of umbilical vein to renal vein (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Dominant dystrophic epidermolysis bullosa with absence of skin	Occurrence	True	Congenital	Inferred relationship	Some	2
Joubert syndrome with congenital hepatic fibrosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
High assimilation pelvis	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital trigger thumb of bilateral hands (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Aorta to right ventricle tunnel	Occurrence	True	Congenital	Inferred relationship	Some	1
Duane anomaly, myopathy, scoliosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Duane anomaly, myopathy, scoliosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Persistent Gartner's duct	Occurrence	False	Congenital	Inferred relationship	Some	2
Melanosis oculi (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Complete cleft hard and soft palate	Occurrence	True	Congenital	Inferred relationship	Some	2
Atrioventricular septal defect with ventricular component under free floating superior bridging leaflet and chords to papillary muscle at right ventricular free wall (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypotrichosis with juvenile macular degeneration syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital retraction of nipple	Occurrence	True	Congenital	Inferred relationship	Some	1
Aortic valve overriding ventricular septum (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Lumbar spina bifida with hydrocephalus - closed	Occurrence	True	Congenital	Inferred relationship	Some	1
Persisting fifth aortic arch with double barrell arch (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Autosomal dominant epidermolysis bullosa simplex (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital diaphragmatic hernia	Occurrence	True	Congenital	Inferred relationship	Some	2
Cutis laxa, autosomal dominant	Occurrence	True	Congenital	Inferred relationship	Some	1
Paravaginal cyst arising in mesonephric duct	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)