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
Lutembacher's syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Persistent ostium secundum	Occurrence	True	Congenital	Inferred relationship	Some	1
Bronchopulmonary collateral artery	Occurrence	True	Congenital	Inferred relationship	Some	1
Cerebral-retinal arteriovenous aneurysm (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Joubert syndrome with Jeune asphyxiating thoracic dystrophy	Occurrence	True	Congenital	Inferred relationship	Some	1
Joubert syndrome with Jeune asphyxiating thoracic dystrophy	Occurrence	True	Congenital	Inferred relationship	Some	3
Joubert syndrome with Jeune asphyxiating thoracic dystrophy	Occurrence	True	Congenital	Inferred relationship	Some	2
Hypoplasia of left ventricular inflow tract	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Palmoplantar keratoderma with clinodactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Palmoplantar keratoderma with clinodactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Incomplete ossification of presphenoid bone	Occurrence	True	Congenital	Inferred relationship	Some	1
Interrupted left inferior vena cava (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Osteogenesis imperfecta with normal sclerae, dominant form	Occurrence	True	Congenital	Inferred relationship	Some	1
Schimke immuno-osseous dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Temporal encephalocele	Occurrence	True	Congenital	Inferred relationship	Some	2
Eccentric opening of aortic valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Left ventricular outflow tract obstruction due to fibromuscular tunnel (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Ramos Arroyo syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete ossification of basioccipital bone	Occurrence	True	Congenital	Inferred relationship	Some	1
Left inferior vena cava connecting to left atrium and right atrium (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Lethal autosomal recessive epidermolysis bullosa simplex	Occurrence	True	Congenital	Inferred relationship	Some	1
Karsch Neugebauer syndrome	Occurrence	True	Congenital	Inferred relationship	Some	4
Karsch Neugebauer syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
Diastrophic dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Multiple epiphyseal dysplasia tarda type IIIa	Occurrence	True	Congenital	Inferred relationship	Some	1
Anonychia with microcephaly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Autosomal dominant hypophosphatemic rickets	Occurrence	True	Congenital	Inferred relationship	Some	1
Female infertility due to structural congenital anomaly of cervix	Occurrence	True	Congenital	Inferred relationship	Some	1
Native American myopathy	Occurrence	True	Congenital	Inferred relationship	Some	1
Ehlers-Danlos syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Common truncus arteriosus (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Trisomy 10p (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Trisomy 10p (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Upper limb defect with eye and ear abnormalities syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Right ventricular outflow tract obstruction due to abnormal cardiac muscle bands (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Eccentric opening of tricuspid aortic valve (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Mesomelic dysplasia Savarirayan type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Short stature, pituitary and cerebellar defect and small sella turcica syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Nemaline myopathy, late onset type	Occurrence	False	Congenital	Inferred relationship	Some	1
Menkes kinky-hair syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Acrofacial dysostosis Palagonia type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Eichsfeld type congenital muscular dystrophy	Occurrence	True	Congenital	Inferred relationship	Some	1
Aniridia type 2	Occurrence	True	Congenital	Inferred relationship	Some	1
FG syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Lumbar hemivertebra - unbalanced	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital anourethral fistula	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital pyloric antral membrane	Occurrence	True	Congenital	Inferred relationship	Some	1
Right ventricular outflow tract abnormality	Occurrence	True	Congenital	Inferred relationship	Some	1
Simple ureterocele	Occurrence	True	Congenital	Inferred relationship	Some	2
Doubling of uterus with doubling of cervix and vagina	Occurrence	True	Congenital	Inferred relationship	Some	1
Double renal pelvis	Occurrence	True	Congenital	Inferred relationship	Some	1
funktionell ovarialcysta	Occurrence	False	Congenital	Inferred relationship	Some	1
Osteogenesis imperfecta, type IV A (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Mesomelic dysplasia of hypoplastic ulna and fibula type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Chondrodysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Persistent tunica vasculosa lentis	Occurrence	True	Congenital	Inferred relationship	Some	2
Persistent tunica vasculosa lentis	Occurrence	True	Congenital	Inferred relationship	Some	1
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Epidermolysis simplex superficialis	Occurrence	True	Congenital	Inferred relationship	Some	1
Dubin-Johnson syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Nodular renal blastema	Occurrence	True	Congenital	Inferred relationship	Some	1
Matthew Wood syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital pulmonary lymphangiectasis	Occurrence	True	Congenital	Inferred relationship	Some	1
Abnormal connection of hepatic vein to atrium	Occurrence	True	Congenital	Inferred relationship	Some	1
Enamel spur	Occurrence	False	Congenital	Inferred relationship	Some	1
medfödd total alopeci	Occurrence	False	Congenital	Inferred relationship	Some	1
Atelosteogenesis type 1 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Winchester syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Frontoethmoidal encephalocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Hutchinson's triad	Occurrence	True	Congenital	Inferred relationship	Some	2
Hereditary neurocutaneous angiomata (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Distal penile hypospadias	Occurrence	True	Congenital	Inferred relationship	Some	1
Fibular dimelia diplopodia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Renal dysplasia with limb defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Renal dysplasia with limb defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital bilateral internal tibial torsion	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital bilateral internal tibial torsion	Occurrence	True	Congenital	Inferred relationship	Some	2
Spondyloepiphyseal dysplasia tarda Kohn type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleft hard and soft palate with right cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Cleft hard and soft palate with right cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Endosteal hyperostoses with cerebellar hypoplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Left ventricular outflow tract obstruction due to malaligned outlet septum (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Right ventricular muscular infundibular stenosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Completely unroofed coronary sinus defect in left atrium (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Junctional epidermolysis bullosa non-Herlitz type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deaf blind hypopigmentation syndrome Yemenite type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deaf blind hypopigmentation syndrome Yemenite type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
atelosteogenes eller diastrofisk dysplasi	Occurrence	False	Congenital	Inferred relationship	Some	1
Rhizomelic chondrodysplasia punctata syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Rhizomelic chondrodysplasia punctata syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Preductal hypoplasia of aorta	Occurrence	True	Congenital	Inferred relationship	Some	1
Brain malformation, congenital heart disease, postaxial polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Brain malformation, congenital heart disease, postaxial polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Brain malformation, congenital heart disease, postaxial polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Ectodermal dysplasia with hair-nail defect	Occurrence	True	Congenital	Inferred relationship	Some	1

Start Previous Page 275 of 330 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)