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
Choroidal atrophy and alopecia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Choroidal atrophy and alopecia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Choroidal atrophy and alopecia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Hallermann-Streiff syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital obstructive megaureter (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete ossification of arch of sacral vertebra	Occurrence	True	Congenital	Inferred relationship	Some	1
Namaqualand hip dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital stenosis of trachea due to complete rings (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Scrotal hypospadias	Occurrence	False	Congenital	Inferred relationship	Some	1
Polydactyly myopia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Radial polydactyly	Occurrence	True	Congenital	Inferred relationship	Some	1
Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Trichorhinophalangeal syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital branched rib cartilage (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Dandy-Walker syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Robinow syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital suprabulbar paresis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Right ventricle to left of left ventricle (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital absence of anus with fistula	Occurrence	True	Congenital	Inferred relationship	Some	1
Jugular lymphatic obstruction sequence	Occurrence	True	Congenital	Inferred relationship	Some	1
Primary renal dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Male pseudohermaphroditism	Occurrence	True	Congenital	Inferred relationship	Some	1
Spinal cord dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Encephalomyelocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Patella dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Patella dysplasia	Occurrence	False	Congenital	Inferred relationship	Some	2
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Dyggve-Melchior-Clausen syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleft hard palate with right cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hyperphosphatasemia tarda	Occurrence	False	Congenital	Inferred relationship	Some	2
Cervical hemivertebra - unbalanced (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Heart-hand syndrome Slovenian type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Heart-hand syndrome Slovenian type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Stern Lubinsky Durrie syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Stern Lubinsky Durrie syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Axenfeld anomaly	Occurrence	True	Congenital	Inferred relationship	Some	1
Singleton-Merten syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Patent foramen ovale	Occurrence	True	Congenital	Inferred relationship	Some	1
Pelvis shoulder dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Macrocephaly with spastic paraplegia and dysmorphism syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Macrocephaly with spastic paraplegia and dysmorphism syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Humeroulnar synostosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Acrorenal syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete ossification of alisphenoid bone	Occurrence	True	Congenital	Inferred relationship	Some	1
Osteopoikilosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital pulmonary hypoplasia due to prolonged premature rupture of membranes (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Intrahepatic biliary hypoplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Pure gonadal dysgenesis 46,XX	Occurrence	True	Congenital	Inferred relationship	Some	2
Atrioventricular septal defect - ventricular component under superior bridging leaflet	Occurrence	True	Congenital	Inferred relationship	Some	1
Epidermolysis bullosa simplex herpetiformis	Occurrence	True	Congenital	Inferred relationship	Some	1
Hepatomphalocele	Occurrence	True	Congenital	Inferred relationship	Some	1
foster med avsaknad av öppningar i kraniet	Occurrence	False	Congenital	Inferred relationship	Some	1
Renier-Gabreels-Jaspers syndrom	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital contractural arachnodactyly	Occurrence	True	Congenital	Inferred relationship	Some	1
Autosomal recessive distal osteolysis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Autosomal recessive distal osteolysis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Neutropenia, monocytopenia, deafness syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
okulocerebralt dysplastiskt syndrom	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital localised alopecia	Occurrence	True	Congenital	Inferred relationship	Some	1
Idiopathic osteolyses	Occurrence	False	Congenital	Inferred relationship	Some	1
medfött endauralt bråck	Occurrence	False	Congenital	Inferred relationship	Some	1
Fusion of mandibular incisor teeth (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Atresia of pulmonary artery with septal defect	Occurrence	True	Congenital	Inferred relationship	Some	1
Total anomalous pulmonary venous connections of mixed type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Ectopic gastric mucosa	Occurrence	True	Congenital	Inferred relationship	Some	1
Gardner syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete ossification of palatine bone	Occurrence	True	Congenital	Inferred relationship	Some	1
Encephalocystocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Encephalocystocele	Occurrence	True	Congenital	Inferred relationship	Some	2
Brachydactyly and preaxial hallux varus syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Schneckenbecken dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital abnormality of right atrioventricular valve in double inlet ventricle (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Persistent omphalomesenteric artery (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Chondrodysplasia with disorder of sex development syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Chondrodysplasia with disorder of sex development syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Acrofacial dysostosis Kennedy Teebi type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital vesicoureterorenal reflux (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Spina bifida with hydrocephalus	Occurrence	True	Congenital	Inferred relationship	Some	3
Congenital stenosis of trachea due to tracheal web (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Lenz-Majewski hyperostosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Epidermolysis bullosa simplex with mottled pigmentation (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Radioulnar synostosis with developmental delay and hypotonia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Radioulnar synostosis with developmental delay and hypotonia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital transposition of stomach	Occurrence	True	Congenital	Inferred relationship	Some	1
Jackson-Weiss syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Jackson-Weiss syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital arteriovenous fistula rupture	Occurrence	True	Congenital	Inferred relationship	Some	1
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Jarcho-Levin syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
parodontit samtidigt med Chédiak-Higashis syndrom	Occurrence	False	Congenital	Inferred relationship	Some	1
DK phocomelia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
DK phocomelia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Chondrodysplasia punctata, X-linked recessive type	Occurrence	True	Congenital	Inferred relationship	Some	1
Right ventricular fibromuscular infundibular stenosis	Occurrence	False	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)