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
Gnathodiaphyseal dysplasia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cervical spina bifida with hydrocephalus - open	Occurrence	True	Congenital	Inferred relationship	Some	3
Cervical spina bifida with hydrocephalus - open	Occurrence	True	Congenital	Inferred relationship	Some	1
Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Parastremmatic dwarfism (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Complete transposition of great vessels	Occurrence	True	Congenital	Inferred relationship	Some	2
Complete transposition of great vessels	Occurrence	True	Congenital	Inferred relationship	Some	1
Popliteal pterygium syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Shprintzen Goldberg craniosynostosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Shprintzen Goldberg craniosynostosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Taurodontia with absent teeth and sparse hair syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Taurodontia with absent teeth and sparse hair syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Taurodontia with absent teeth and sparse hair syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital pontocerebellar hypoplasia type 8 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Lelis syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Brachydactylous dwarfism Mseleni type	Occurrence	False	Congenital	Inferred relationship	Some	1
Interatrial communication through coronary sinus orifice (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Keratin 14 related epidermolysis bullosa simplex (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete ossification of fibula	Occurrence	True	Congenital	Inferred relationship	Some	1
Imperforate jejunum	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital atrial septal defect (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Lymphedema, atrial septal defect, facial changes syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Lymphedema, atrial septal defect, facial changes syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Joubert syndrome with ocular defect (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
övertaliga rötter	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital broncho-esophageal fistula without atresia	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleft lip and cleft palate with ectodermal dysplasia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Melnick-Needles syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Hemicentric sacral centrum	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital cataract with ataxia and deafness syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Thoracolumbar spina bifida with hydrocephalus - closed	Occurrence	True	Congenital	Inferred relationship	Some	3
Nevus comedonicus	Occurrence	True	Congenital	Inferred relationship	Some	1
Multiple synostosis syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Longitudinal absence of radius AND ulna	Occurrence	True	Congenital	Inferred relationship	Some	1
Longitudinal absence of radius AND ulna	Occurrence	True	Congenital	Inferred relationship	Some	2
Port-wine stain associated with spinal dysraphism (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Port-wine stain associated with spinal dysraphism (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Flynn-Aird syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Curry-Hall syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Marshall syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Acrocephalopolysyndactyly type IV (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Acrocephalopolysyndactyly type IV (disorder)	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	1
Immuno-osseous dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Schmitt Gillenwater Kelly syndrome	Occurrence	True	Congenital	Inferred relationship	Some	4
Hypohidrosis with neurolabyrinthitis	Occurrence	True	Congenital	Inferred relationship	Some	2
Manus valga	Occurrence	False	Congenital	Inferred relationship	Some	2
Spina bifida aperta of thoracic spine (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Spina bifida aperta of thoracic spine (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypohidrotic X-linked ectodermal dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Smith-Fineman-Myers syndrom	Occurrence	False	Congenital	Inferred relationship	Some	1
Carbohydrate sulfotransferase 3 related skeletal dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Dappled diaphyseal dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cutis gyrata syndrome of Beare and Stevenson	Occurrence	True	Congenital	Inferred relationship	Some	1
Juvenile fucosidosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital stricture of osseous meatus	Occurrence	True	Congenital	Inferred relationship	Some	1
Familial multiple café-au-lait macules without neurofibromatosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Syndromic recessive X-linked ichthyosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
ossös syndaktyli av andra till fjärde tåmellanrummen	Occurrence	False	Congenital	Inferred relationship	Some	1
Mobile kidney	Occurrence	True	Congenital	Inferred relationship	Some	1
Hydrocephalus, cardiac malformation, dense bone syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Hydrocephalus, cardiac malformation, dense bone syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Vascular loops of inner ear	Occurrence	True	Congenital	Inferred relationship	Some	1
Camptodactyly taurinuria syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Craniopagus parasiticus	Occurrence	True	Congenital	Inferred relationship	Some	1
brakyolmi, Hobaek-typ	Occurrence	False	Congenital	Inferred relationship	Some	1
Omphalocele with obstruction	Occurrence	True	Congenital	Inferred relationship	Some	3
Dicephalus tripus tribrachius	Occurrence	True	Congenital	Inferred relationship	Some	1
Deafness with skeletal dysplasia and lip granuloma syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deafness with skeletal dysplasia and lip granuloma syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Pseudohypoparathyroidism type I A	Occurrence	True	Congenital	Inferred relationship	Some	1
Spondyloepimetaphyseal dysplasia with joint laxity	Occurrence	True	Congenital	Inferred relationship	Some	1
Greig cephalopolysyndactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Bosley Salih Alorainy syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Neurofaciodigitorenal syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Neurofaciodigitorenal syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Pili annulati	Occurrence	True	Congenital	Inferred relationship	Some	1
Mesomelic dysplasia Kantaputra type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital microgastria with limb reduction defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleidorhizomelic syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Seckel syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Seckel syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Craniopagus occipitalis	Occurrence	True	Congenital	Inferred relationship	Some	1
Arthrogryposis hyperkeratosis syndrome lethal form (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Arthrogryposis hyperkeratosis syndrome lethal form (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital vascular malformation due to inherited syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypertaurodontism	Occurrence	False	Congenital	Inferred relationship	Some	1
Left ventricular outflow tract obstruction due to diaphragm (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Vertical retraction syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Microgyria	Occurrence	True	Congenital	Inferred relationship	Some	1
Severe generalized recessive dystrophic epidermolysis bullosa (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital micrognathism	Occurrence	True	Congenital	Inferred relationship	Some	1
Patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hand-foot-genital syndrome	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)