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
Congenital vascular anomaly of lower eyelid	Occurrence	True	Congenital	Inferred relationship	Some	1
Chronic granulomatous disease (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Temporal encephalocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Lumbar meningomyelocele	Occurrence	True	Congenital	Inferred relationship	Some	3
Lumbar meningomyelocele	Occurrence	False	Congenital	Inferred relationship	Some	2
Lumbar meningomyelocele	Occurrence	True	Congenital	Inferred relationship	Some	4
Parietal encephalocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital cerebral meningocele	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital cerebral meningocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Spina bifida of lumbar region	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital protrusion of tongue	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital sacral meningocele with conotruncal heart defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Low lumbar myelomeningocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Cervical myelocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Cervical myelocele	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital cerebral hernia	Occurrence	True	Congenital	Inferred relationship	Some	1
kranialt hydromeningocele	Occurrence	False	Congenital	Inferred relationship	Some	1
Thoracic myelocele	Occurrence	True	Congenital	Inferred relationship	Some	2
Dens evaginatus	Occurrence	False	Congenital	Inferred relationship	Some	1
High lumbar myelomeningocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Lumbar myelocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Lumbar myelocele	Occurrence	True	Congenital	Inferred relationship	Some	2
Lumbar spina bifida without hydrocephalus - closed (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Thoracic meningomyelocele	Occurrence	False	Congenital	Inferred relationship	Some	2
Thoracic meningomyelocele	Occurrence	True	Congenital	Inferred relationship	Some	3
Thoracic meningomyelocele	Occurrence	True	Congenital	Inferred relationship	Some	4
Congenital abnormal long growth of bile duct	Occurrence	True	Congenital	Inferred relationship	Some	1
Cervical meningomyelocele	Occurrence	False	Congenital	Inferred relationship	Some	2
Cervical meningomyelocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Cervical meningomyelocele	Occurrence	True	Congenital	Inferred relationship	Some	4
Bilateral medullary sponge kidney (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital onychauxis	Occurrence	True	Congenital	Inferred relationship	Some	1
Navajo neurohepatopathy	Occurrence	True	Congenital	Inferred relationship	Some	2
Navajo neurohepatopathy	Occurrence	True	Congenital	Inferred relationship	Some	1
Familial congenital mirror movements	Occurrence	True	Congenital	Inferred relationship	Some	1
Antecubital pterygium syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Pulmonary valve agenesis, intact ventricular septum, persistent ductus arteriosus syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Pulmonary valve agenesis, intact ventricular septum, persistent ductus arteriosus syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Craniorhiny (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Craniorhiny (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Craniorhiny (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation	Occurrence	True	Congenital	Inferred relationship	Some	3
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation	Occurrence	True	Congenital	Inferred relationship	Some	2
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation	Occurrence	True	Congenital	Inferred relationship	Some	1
Developmental dislocation of ankle and/or foot (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Developmental dislocation of ankle and/or foot (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Developmental dislocation of joint of shoulder region (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Developmental dislocation of joint of shoulder region (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital single renal cyst (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Ectopic artery (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Autosomal recessive cutis laxa type 2A (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Autosomal recessive cutis laxa type 2A (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Posterior fossa arachnoid cyst (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Atrioventricular septal defect with atrioventricular valve regurgitation through right anterosuperior inferior mural commissure (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrioventricular septal defect with atrioventricular valve regurgitation through right anterosuperior superior bridging leaflet commissure (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrioventricular septal defect with atrioventricular valve regurgitation through right inferior bridging leaflet inferior mural commissure (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital cystic disease of liver	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrioventricular septal defect with atrioventricular valve regurgitation through left septal commissure (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrioventricular septal defect with atrioventricular valve regurgitation through left superior bridging leaflet lateral mural commissure (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrioventricular septal defect with atrioventricular valve regurgitation through right septal commissure (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital vesicoureterorenal reflux, bilateral	Occurrence	True	Congenital	Inferred relationship	Some	4
Atrioventricular septal defect with atrioventricular valve regurgitation through left inferior bridging leaflet lateral mural commissure (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrioventricular septal defect with atrioventricular valve regurgitation (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Multiple congenital anomalies, hypotonia, seizures syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Multiple congenital anomalies, hypotonia, seizures syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Multiple congenital anomalies, hypotonia, seizures syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Muscle eye brain disease with bilateral multicystic leukodystrophy	Occurrence	True	Congenital	Inferred relationship	Some	4
Muscle eye brain disease with bilateral multicystic leukodystrophy	Occurrence	True	Congenital	Inferred relationship	Some	2
Cobblestone lissencephaly without muscular or ocular involvement (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Autosomal recessive spastic paraplegia type 24	Occurrence	False	Congenital	Inferred relationship	Some	1
Autosomal dominant spastic paraplegia type 8	Occurrence	False	Congenital	Inferred relationship	Some	1
Lissencephaly with cerebellar hypoplasia type E	Occurrence	True	Congenital	Inferred relationship	Some	1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypertrophic Meckel's diverticulum	Occurrence	True	Congenital	Inferred relationship	Some	1
Pachyonychia congenita syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Obesity due to leptin receptor gene deficiency	Occurrence	True	Congenital	Inferred relationship	Some	1
Obesity due to leptin receptor gene deficiency	Occurrence	True	Congenital	Inferred relationship	Some	2
Branchial cleft sinus and fistula	Occurrence	True	Congenital	Inferred relationship	Some	2
Fistula of branchial cleft	Occurrence	True	Congenital	Inferred relationship	Some	1
Aneurysm osteoarthritis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Aneurysm osteoarthritis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Fordyce's disease	Occurrence	False	Congenital	Inferred relationship	Some	1
Fordyce spots of lips (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Bilateral multicystic renal dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Distal arthrogryposis type 4 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Lethal congenital contracture syndrome type 2 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital anomaly of right optic disc	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital anomaly of bilateral optic discs (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital anomaly of bilateral optic discs (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital anomaly of left optic disc (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Fistula colli congenita	Occurrence	True	Congenital	Inferred relationship	Some	1
Arthrogryposis and ectodermal dysplasia syndrome	Occurrence	True	Congenital	Inferred relationship	Some	5
Arthrogryposis and ectodermal dysplasia syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Arthrogryposis and ectodermal dysplasia syndrome	Occurrence	True	Congenital	Inferred relationship	Some	4
Arthrogryposis and ectodermal dysplasia syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
Congenital systemic arteriovenous fistula	Occurrence	True	Congenital	Inferred relationship	Some	1
Microphthalmos of right eye	Occurrence	True	Congenital	Inferred relationship	Some	1

Start Previous Page 296 of 322 Next End

This concept is not in any reference sets

Back to Start

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)