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
partiellt bilateralt kluven gom med kluven läpp	Occurrence	False	Congenital	Inferred relationship	Some	3
Central complete cleft palate with cleft lip	Occurrence	True	Congenital	Inferred relationship	Some	1
Central incomplete cleft palate with cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleft hard palate with cleft lip, bilateral	Occurrence	True	Congenital	Inferred relationship	Some	2
keilopalatoschis	Occurrence	False	Congenital	Inferred relationship	Some	1
Bilateral incomplete cleft lip and alveolus	Occurrence	True	Congenital	Inferred relationship	Some	1
Complete cleft hard and soft palate	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleft upper lip, upper jaw AND palate	Occurrence	True	Congenital	Inferred relationship	Some	1
Cheilognathouranoschisis	Occurrence	True	Congenital	Inferred relationship	Some	1
keilognatopalatoschis	Occurrence	False	Congenital	Inferred relationship	Some	1
Component of oligomeric golgi complex 7 congenital disorder of glycosylation (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Component of oligomeric golgi complex 8 congenital disorder of glycosylation (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Coloboma of macula with brachydactyly type B syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Coloboma of macula with brachydactyly type B syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Coloboma of macula with brachydactyly type B syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Global developmental delay, osteopenia, ectodermal defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Global developmental delay, osteopenia, ectodermal defect syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Glossopalatine ankylosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Glossopalatine ankylosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Glossopalatine ankylosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Glossopalatine ankylosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Goldberg Shprintzen megacolon syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	8
Goldberg Shprintzen megacolon syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	9
Goldberg Shprintzen megacolon syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	10
Goldberg Shprintzen megacolon syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	11
Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Hydrocephalus, cardiac malformation, dense bone syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Hydrocephalus, cardiac malformation, dense bone syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Hydrocephalus, cardiac malformation, dense bone syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Blepharoptosis, myopia, ectopia lentis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Blepharoptosis, myopia, ectopia lentis syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Bifid nose, anorectal anomaly, renal anomaly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Brain malformation, congenital heart disease, postaxial polydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Brain malformation, congenital heart disease, postaxial polydactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Brain malformation, congenital heart disease, postaxial polydactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Brain malformation, congenital heart disease, postaxial polydactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Branchiogenic deafness syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Intellectual disability, epilepsy, bulbous nose syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hidrotic ectodermal dysplasia Halal type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Hidrotic ectodermal dysplasia Halal type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Hidrotic ectodermal dysplasia Halal type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Hidrotic ectodermal dysplasia Halal type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Hirschsprung disease with deafness and polydactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	8
Hirschsprung disease with deafness and polydactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	9
Hirschsprung disease with type D brachydactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Hirschsprung disease with type D brachydactyly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	8
Hirschsprung disease with nail hypoplasia and dysmorphism (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	8
Hirschsprung disease with nail hypoplasia and dysmorphism (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	9
Hirschsprung disease with nail hypoplasia and dysmorphism (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	10
Holmes-Gangs syndrom	Occurrence	False	Congenital	Inferred relationship	Some	1
Hunter McAlpine craniosynostosis syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Hydrocephalus with obesity and hypogonadism syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
infektion som orsakar kongenital anomali	Occurrence	False	Congenital	Inferred relationship	Some	1
Hypertrichosis and acromegaloid facial appearance syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Hypertrichosis and acromegaloid facial appearance syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Hypomandibular faciocranial dysostosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Hypomandibular faciocranial dysostosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	5
Juberg Hayward syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Juberg Hayward syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Juberg Hayward syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Juberg Marsidi syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Microphthalmia with brain and digit anomaly (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Microphthalmia with linear skin defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Microphthalmia with linear skin defect syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Congenital microgastria with limb reduction defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital microgastria with limb reduction defect syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Microduplication Xp11.22p11.23 syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Radioulnar synostosis with developmental delay and hypotonia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Radioulnar synostosis with developmental delay and hypotonia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Puerto Rican infant hypotonia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Puerto Rican infant hypotonia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Puerto Rican infant hypotonia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Scalp, ear, nipple syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Scalp, ear, nipple syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Scalp, ear, nipple syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Scalp, ear, nipple syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Schilbach Rott syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Schilbach Rott syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Robinow-liknande syndrom	Occurrence	False	Congenital	Inferred relationship	Some	4
Robinow-liknande syndrom	Occurrence	False	Congenital	Inferred relationship	Some	5
Robinow-liknande syndrom	Occurrence	False	Congenital	Inferred relationship	Some	6
Uranostaphyloschisis with cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleft of soft palate and bilateral cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleft of soft palate and cleft lip (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hip dysplasia Beukes type (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Bilateral microtia with deafness and cleft palate syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Bilateral microtia with deafness and cleft palate syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Bilateral microtia with deafness and cleft palate syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Blepharonasofacial malformation syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3

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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)