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
Ehlers-Danlos syndrome, hydroxylysine-deficient	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital obstruction of small intestine	Occurrence	True	Congenital	Inferred relationship	Some	1
Robinson nail dystrophy-deafness syndrome	Occurrence	True	Congenital	Inferred relationship	Some	6
Coarctation of pulmonary artery	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital syphilitic periostitis	Occurrence	True	Congenital	Inferred relationship	Some	1
Ascher's syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Ascher's syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Schwartz-Jampel syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Schwartz-Jampel syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
Hypophosphataemic rickets with nephrotic-glycosuric dwarfism	Occurrence	True	Congenital	Inferred relationship	Some	3
Autosomal dominant hypophosphatemic rickets	Occurrence	False	Congenital	Inferred relationship	Some	3
Autosomal dominant hypophosphataemic bone disease	Occurrence	False	Congenital	Inferred relationship	Some	3
Mucopolysaccharidosis, MPS-IV-B	Occurrence	True	Congenital	Inferred relationship	Some	1
Juvenile hyaline fibromatosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Juvenile elastofibromatosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypohidrotic X-linked ectodermal dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	4
Roselli-Gulienetti ectodermal dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	4
Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	4
Basan syndrome	Occurrence	True	Congenital	Inferred relationship	Some	4
Greither type of ectodermal dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	4
Tricho-onychodental dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	4
Schoepf-Schulz-Passage syndrome	Occurrence	True	Congenital	Inferred relationship	Some	4
Odonto-onychial dysplasia with alopecia	Occurrence	True	Congenital	Inferred relationship	Some	6
Fried's tooth and nail syndrome	Occurrence	True	Congenital	Inferred relationship	Some	4
Dermodental dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	4
Salamon's syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Ectodermal dysplasia, syndactyly and pili torti	Occurrence	True	Congenital	Inferred relationship	Some	4
Dwarfism, alopecia, pseudoanodontia, cutis laxa	Occurrence	True	Congenital	Inferred relationship	Some	4
Hypohidrosis-diabetes insipidus syndrome	Occurrence	True	Congenital	Inferred relationship	Some	5
Hypohidrosis-diabetes insipidus syndrome	Occurrence	True	Congenital	Inferred relationship	Some	7
Odontotrichomelic syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Dento-oculocutaneous syndrome	Occurrence	True	Congenital	Inferred relationship	Some	4
Hair follicle naevus	Occurrence	True	Congenital	Inferred relationship	Some	1
Persistent vertical vein	Occurrence	True	Congenital	Inferred relationship	Some	1
Right hypoplastic heart syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Curry-Hall syndrome	Occurrence	True	Congenital	Inferred relationship	Some	4
Dental midlines coincident and incorrect	Occurrence	False	Congenital	Inferred relationship	Some	2
Goniodysgenesis	Occurrence	True	Congenital	Inferred relationship	Some	1
Defect of telencephalic division	Occurrence	True	Congenital	Inferred relationship	Some	1
Hydranencephaly with proliferative vasculopathy	Occurrence	True	Congenital	Inferred relationship	Some	1
Schizencephaly	Occurrence	True	Congenital	Inferred relationship	Some	1
Double inlet right ventricle	Occurrence	True	Congenital	Inferred relationship	Some	1
Double inlet left ventricle	Occurrence	True	Congenital	Inferred relationship	Some	1
Right sided atrium connecting to ventricle of indeterminate morphology	Occurrence	True	Congenital	Inferred relationship	Some	1
Double outlet right ventricle with subaortic ventricular septal defect	Occurrence	True	Congenital	Inferred relationship	Some	1
Double outlet right ventricle with noncommitted ventricular septal defect	Occurrence	True	Congenital	Inferred relationship	Some	1
Double outlet right ventricle with doubly committed ventricular septal defect	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrial septal defect through coronary sinus orifice	Occurrence	True	Congenital	Inferred relationship	Some	2
Double orifice of tricuspid valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Ebstein-like downward displacement of mitral valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Double outlet left atrium	Occurrence	True	Congenital	Inferred relationship	Some	1
Ebstein's anomaly of right atrioventricular valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Ebstein's anomaly of left atrioventricular valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Megacystis, microcolon, hypoperistalsis syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Megacystis, microcolon, hypoperistalsis syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Neuronal intestinal dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
bristande nedsjunkning av testikel, dubbelsidig	Occurrence	False	Congenital	Inferred relationship	Some	2
bristande nedsjunkning av testikel, dubbelsidig	Occurrence	False	Congenital	Inferred relationship	Some	1
Ectopic ureterocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Phocomelia of upper limb (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Desbuquois syndrome	Occurrence	True	Congenital	Inferred relationship	Some	4
Axial osteosclerosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Francois syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Francois syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
Salmon patch naevus	Occurrence	True	Congenital	Inferred relationship	Some	1
Vitellointestinal band	Occurrence	True	Congenital	Inferred relationship	Some	1
Persistent descending vein	Occurrence	True	Congenital	Inferred relationship	Some	1
Vestigial gastrointestinal remnant	Occurrence	True	Congenital	Inferred relationship	Some	1
hydromyelocele med hydrocefalus	Occurrence	False	Congenital	Inferred relationship	Some	1
hydromyelocele med hydrocefalus	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenital syphilitic rhinitis	Occurrence	True	Congenital	Inferred relationship	Some	1
Totally absent pericardium	Occurrence	True	Congenital	Inferred relationship	Some	1
Dilatation of tricuspid annulus (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Overriding tricuspid valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Overriding mitral valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Undescended testes - bilateral	Occurrence	True	Congenital	Inferred relationship	Some	1
Undescended testes - bilateral	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital calyceal diverticulum	Occurrence	True	Congenital	Inferred relationship	Some	1
Chiari's network	Occurrence	True	Congenital	Inferred relationship	Some	1
Right ventricular outflow tract absent	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital duodenal obstruction due to malrotation of intestine	Occurrence	True	Congenital	Inferred relationship	Some	1
Ectodermal dysplasia with hair-tooth-nail-sweating defect	Occurrence	True	Congenital	Inferred relationship	Some	4
Ectodermal dysplasia with hair-tooth-nail defects	Occurrence	True	Congenital	Inferred relationship	Some	4
Ectodermal dysplasia with tooth-nail defects	Occurrence	True	Congenital	Inferred relationship	Some	4
Dentate dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Isomerism of right atrial appendage (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Isomerism of left atrial appendage (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Two chambered right ventricle	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital coronary artery calcification	Occurrence	True	Congenital	Inferred relationship	Some	1
Trilobular liver	Occurrence	True	Congenital	Inferred relationship	Some	1
Short preputial frenulum	Occurrence	True	Congenital	Inferred relationship	Some	1
Overgrowth of upper limb	Occurrence	True	Congenital	Inferred relationship	Some	1
Vascular birthmark	Occurrence	True	Congenital	Inferred relationship	Some	1
Persistent Gartner's duct	Occurrence	True	Congenital	Inferred relationship	Some	1
Ectopic gray matter	Occurrence	True	Congenital	Inferred relationship	Some	1
Intralobar bronchopulmonary sequestration	Occurrence	True	Congenital	Inferred relationship	Some	1
Bilobed right lung	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital subluxation of hip	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital hydroureter	Occurrence	True	Congenital	Inferred relationship	Some	1
hornhinnefragilitet, keratoglobus, blå senhinna och ledöverrörlighet	Occurrence	False	Congenital	Inferred relationship	Some	2
Anomalous pulmonary venous drainage to hepatic veins	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)