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
Spastic paraplegia, nephritis, deafness syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Spastic paraplegia, glaucoma, intellectual disability syndrome	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital conductive hearing loss	Occurrence	False	Congenital	Inferred relationship	Some	3
Congenital hallux valgus of left great toe (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital hallux valgus of right great toe (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
medfödd triggertumme på båda händerna	Occurrence	False	Congenital	Inferred relationship	Some	2
medfödd triggertumme på båda händerna	Occurrence	False	Congenital	Inferred relationship	Some	3
Congenital trigger finger of right hand	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital trigger finger of left hand (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital coloboma of macula lutea	Occurrence	True	Congenital	Inferred relationship	Some	1
Tibio-fibular synostosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Bilateral multicystic renal dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Bilateral multicystic renal dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Congenital hypoplasia of odontoid process of axis	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypoplasia of sacrum (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital absence of forearm and hand	Occurrence	False	Congenital	Inferred relationship	Some	4
Congenital absence of forearm and hand	Occurrence	False	Congenital	Inferred relationship	Some	5
Congenital absence of forearm and hand	Occurrence	False	Congenital	Inferred relationship	Some	6
Autosomal dominant hereditary spastic paraplegia	Occurrence	False	Congenital	Inferred relationship	Some	2
Longitudinal deficiency of upper and lower limbs	Occurrence	True	Congenital	Inferred relationship	Some	2
Longitudinal deficiency of upper and lower limbs	Occurrence	False	Congenital	Inferred relationship	Some	3
Congenital mixed conductive and sensorineural hearing loss	Occurrence	False	Congenital	Inferred relationship	Some	2
Multicystic renal dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Lop ear deformity	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital hyperplasia of lung	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital stenosis of large intestine (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital anomaly of atrioventricular valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital anomaly of atrioventricular septum	Occurrence	True	Congenital	Inferred relationship	Some	1
Aplasia of patella	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital thrombocytopenia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Pericarditis secondary to Mulibrey nanism	Occurrence	False	Congenital	Inferred relationship	Some	4
Congenital absence of right mandibular condyle	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital absence of left mandibular condyle	Occurrence	True	Congenital	Inferred relationship	Some	1
Pseudovaginal perineoscrotal hypospadias	Occurrence	False	Congenital	Inferred relationship	Some	4
Retinitis pigmentosa-deafness syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Retinitis pigmentosa-deafness-ataxia syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Goldenhar syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Gorlin-Chaudhry-Moss syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Oculo-palato-digital syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Oculo-palato-digital syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Usher syndrome type 1	Occurrence	True	Congenital	Inferred relationship	Some	2
Usher syndrome type 2 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
hypogonadism, diabetes mellitus, alopeci, psykisk utvecklingsstörning och elektrokardiografiska avvikelser	Occurrence	False	Congenital	Inferred relationship	Some	1
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness	Occurrence	True	Congenital	Inferred relationship	Some	4
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness	Occurrence	True	Congenital	Inferred relationship	Some	5
Oculodento-osseous dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Oculodento-osseous dysplasia	Occurrence	False	Congenital	Inferred relationship	Some	3
Floating-Harbour syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Kabuki make-up syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Renal coloboma syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Renal coloboma syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Solitary median maxillary central incisor syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Solitary median maxillary central incisor syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
Francois syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Peroxisome biogenesis disorder	Occurrence	True	Congenital	Inferred relationship	Some	1
Isolated follicle stimulating hormone deficiency	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital cyst of orbit (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
multipel lokalisation av icke-benbildande fibromatos	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital cardiovascular disorder (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital bronchogenic cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital anomaly of zonula	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleft hard palate with left cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Cleft hard palate with left cleft lip (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Cleft hard palate with right cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Cleft hard palate with right cleft lip (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Cleft soft palate with left cleft lip	Occurrence	True	Congenital	Inferred relationship	Some	2
Cleft soft palate with left cleft lip	Occurrence	False	Congenital	Inferred relationship	Some	3
Cleft soft palate with right cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Cleft soft palate with right cleft lip (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Cleft hard and soft palate with left cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Cleft hard and soft palate with left cleft lip (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Cleft hard and soft palate with left cleft lip (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Cleft hard and soft palate with right cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Cleft hard and soft palate with right cleft lip (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Cleft hard and soft palate with right cleft lip (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Cleft palate with left cleft lip	Occurrence	True	Congenital	Inferred relationship	Some	2
Cleft palate with left cleft lip	Occurrence	False	Congenital	Inferred relationship	Some	3
Cleft palate with right cleft lip	Occurrence	True	Congenital	Inferred relationship	Some	2
Cleft palate with right cleft lip	Occurrence	False	Congenital	Inferred relationship	Some	3
Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral artery	Occurrence	False	Congenital	Inferred relationship	Some	7
Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral artery	Occurrence	False	Congenital	Inferred relationship	Some	8
Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral artery	Occurrence	False	Congenital	Inferred relationship	Some	9
Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral artery	Occurrence	False	Congenital	Inferred relationship	Some	10
Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral artery	Occurrence	False	Congenital	Inferred relationship	Some	11
Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral artery	Occurrence	False	Congenital	Inferred relationship	Some	12
Haemodynamically insignificant ventricular septal defect	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital anomaly of great vessel	Occurrence	True	Congenital	Inferred relationship	Some	1
Double outlet right ventricle with subaortic or doubly committed ventricular septal defect without pulmonary stenosis - ventricular septal defect type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Double outlet right ventricle with subaortic or doubly committed ventricular septal defect without pulmonary stenosis - ventricular septal defect type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Common arterial trunk with aortic dominance (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Common arterial trunk with aortic dominance (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Common arterial trunk with pulmonary dominance co-occurrent with interrupted aortic arch (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Common arterial trunk with pulmonary dominance co-occurrent with interrupted aortic arch (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Common arterial trunk with pulmonary dominance co-occurrent with interrupted aortic arch (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Common arterial trunk with pulmonary dominance co-occurrent with interrupted aortic arch (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Congenital dysplasia of tricuspid valve	Occurrence	True	Congenital	Inferred relationship	Some	1
perforation av tarmen hos intrauterint foster med medfödd stenos i tarmkanalen	Occurrence	False	Congenital	Inferred relationship	Some	4
Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Congenital obstructive hydrocephalus	Occurrence	True	Congenital	Inferred relationship	Some	1
Microphthalmic socket (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleft hard palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4

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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)