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
Trigonocephaly with broad thumb syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	8
Trigonocephaly with broad thumb syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	9
Triphalangeal thumb and polysyndactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Triphalangeal thumb and polysyndactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Triphalangeal thumb with brachyectrodactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Triphalangeal thumb with brachyectrodactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Haddad syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Haim Munk syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Autosomal dominant limb girdle muscular dystrophy type 1A (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
autosomalt dominant muskeldystrofi i skulder-bäckengördel, typ 1C	Occurrence	False	Congenital	Inferred relationship	Some	2
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Autosomal dominant limb girdle muscular dystrophy type 1E (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Autosomal dominant limb girdle muscular dystrophy type 1F (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Haim Munk syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Woolly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome	Occurrence	False	Congenital	Inferred relationship	Some	7
Timothy syndrome type 2 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital anomaly of right ear (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital atresia of right external ear (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Uterus bicornis bicollis with blind hemi-vagina (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Uterus bicornis bicollis with patent cervix and vagina	Occurrence	True	Congenital	Inferred relationship	Some	1
Bilateral congenital absence of ovary (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Bilateral congenital absence of ovary (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Bilateral congenital absence of fallopian tube (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Bilateral congenital absence of fallopian tube (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Primary renal dysplasia (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Secondary renal dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Bilateral secondary renal dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Bilateral secondary renal dysplasia (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Congenital hemorrhagic renal cyst (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Bilateral medullary sponge kidney (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Bilateral congenital primary hydronephrosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Complete duplication of urethra (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Partial duplication of urethra (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital atresia and stenosis of ureter (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital atresia and stenosis of ureter (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Congenital absence of bladder and urethra (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital absence of bladder and urethra (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Atresia of the esophagus without tracheoesophageal fistula	Occurrence	True	Congenital	Inferred relationship	Some	1
Arteriovenous malformation of stomach (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Arteriovenous malformation of duodenum (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Congenital diverticulum of duodenum (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital malrotation of duodenum (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Biemond syndrome type 2 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hyperinsulinism due to focal adenomatous hyperplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
17p13.3 microduplication syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Intractable diarrhea with choanal atresia and eye anomaly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Intractable diarrhea with choanal atresia and eye anomaly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Intractable diarrhea with choanal atresia and eye anomaly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Congenital tracheobiliary fistula (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital tracheobiliary fistula (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Acrofrontofacionasal dysostosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Acrofrontofacionasal dysostosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Acrofrontofacionasal dysostosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Acrootoocular syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Acrootoocular syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Acropectoral syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Acropectoral syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
akropektororenal dysplasi	Occurrence	False	Congenital	Inferred relationship	Some	3
akropektororenal dysplasi	Occurrence	False	Congenital	Inferred relationship	Some	4
akropektororenal dysplasi	Occurrence	False	Congenital	Inferred relationship	Some	5
Acrorenal mandibular syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Acrorenal mandibular syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Acrorenal mandibular syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Acrorenoocular syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Acrorenoocular syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Acrorenoocular syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Acrocapitofemoral dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Acrocephalopolydactyly (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Acrocephalopolydactyly (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Acrocraniofacial dysostosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Acrocraniofacial dysostosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Acrocraniofacial dysostosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Acromegaloid facial appearance syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Acromegaloid facial appearance syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Acropectorovertebral dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Acropectorovertebral dysplasia (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Acropectorovertebral dysplasia (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Acropectorovertebral dysplasia (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Acrorenal syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Acrorenal syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Doughnut lesion of calvaria and bone fragility syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Doughnut lesion of calvaria and bone fragility syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Campomelia Cumming type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Campomelia Cumming type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	8
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	9
Camptodactyly and tall stature with scoliosis and hearing loss syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Camptodactyly and tall stature with scoliosis and hearing loss syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Camptodactyly and tall stature with scoliosis and hearing loss syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Camptodactyly syndrome Guadalajara type 1 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Camptodactyly syndrome Guadalajara type 1 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Camptodactyly syndrome Guadalajara type 1 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Camptodactyly syndrome Guadalajara type 2 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Camptodactyly syndrome Guadalajara type 2 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Camptodactyly syndrome Guadalajara type 2 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Cardiac anomaly and heterotaxy syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cardiocranial syndrome Pfeiffer type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2

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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)