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
splenomegali samtidig med och orsakad av inlagringssjukdom	Occurrence	False	Congenital	Inferred relationship	Some	1
Transient abnormal myelopoiesis co-occurrent with Down syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital dacryocele (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Common atrioventricular junction (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 2 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of long arm of chromosome 2 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of part of long arm of chromosome 2 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Deletion of part of short arm of chromosome 2 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of part of short arm of chromosome 2 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Deletion of part of chromosome 3 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of long arm of chromosome 3 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of part of long arm of chromosome 3 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Deletion of part of chromosome 4 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 5 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of long arm of chromosome 5 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of part of long arm of chromosome 5 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Deletion of part of chromosome 6 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of long arm of chromosome 6 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of part of long arm of chromosome 6 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Deletion of part of short arm of chromosome 6 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Deletion of part of short arm of chromosome 6 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Deletion of part of chromosome 7 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 8 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 9 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 10 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 11 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 12 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of long arm of chromosome 12 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of part of long arm of chromosome 12 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Deletion of part of chromosome 13 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 14 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 15 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 16 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of short arm of chromosome 16 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of part of short arm of chromosome 16 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Deletion of part of chromosome 17 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of short arm of chromosome 17 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of part of short arm of chromosome 17 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Deletion of part of chromosome 18 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 19 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of long arm of chromosome 19 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of long arm of chromosome 19 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Deletion of short arm of chromosome 19 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of short arm of chromosome 19 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Deletion of part of chromosome 20 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of long arm of chromosome 20 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of part of long arm of chromosome 20 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Deletion of part of short arm of chromosome 20 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deletion of part of short arm of chromosome 20 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Deletion of part of chromosome 21 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Deletion of part of chromosome 22 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Uniparental disomy (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital malposition of eyelid (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Dystopia canthorum (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Autosomal dominant spastic paraplegia type 10 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Autosomal dominant spastic paraplegia type 6 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Ichthyosis, oral and digital anomalies syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
Ichthyosis, oral and digital anomalies syndrome	Occurrence	False	Congenital	Inferred relationship	Some	4
Ichthyosis, oral and digital anomalies syndrome	Occurrence	False	Congenital	Inferred relationship	Some	5
Mitochondrial myopathy, lactic acidosis, deafness syndrome	Occurrence	False	Congenital	Inferred relationship	Some	4
Congenital cataract ichthyosis syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital cataract ichthyosis syndrome	Occurrence	False	Congenital	Inferred relationship	Some	3
Ectodermal dysplasia and sensorineural deafness syndrome	Occurrence	False	Congenital	Inferred relationship	Some	5
Ectodermal dysplasia and sensorineural deafness syndrome	Occurrence	False	Congenital	Inferred relationship	Some	6
Osteopenia, intellectual disability, sparse hair syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Osteopenia, intellectual disability, sparse hair syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Osteopenia, intellectual disability, sparse hair syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Symphalangism with multiple anomalies of hands and feet syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Brachydactyly and distal symphalangism syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Brachydactyly and distal symphalangism syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Brachydactyly and preaxial hallux varus syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Brachydactyly and preaxial hallux varus syndrome	Occurrence	False	Congenital	Inferred relationship	Some	3
Spastic paraplegia with precocious puberty syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Branchial dysplasia, intellectual disability, inguinal hernia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Familial infantile myasthenia	Occurrence	True	Congenital	Inferred relationship	Some	1
Acetylcholine resynthesis deficiency (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital secondary hydronephrosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome	Occurrence	False	Congenital	Inferred relationship	Some	5
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome	Occurrence	False	Congenital	Inferred relationship	Some	6
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome	Occurrence	False	Congenital	Inferred relationship	Some	7
Autosomal dominant spastic paraplegia type 29 (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Congenital hypoplasia of ulna and split foot syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Congenital hypoplasia of ulna and split foot syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Congenital hypoplasia of ulna and split foot syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Epilepsy telangiectasia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Epilepsy telangiectasia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Epilepsy telangiectasia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
Epilepsy telangiectasia syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	8
Spinocerebellar ataxia dysmorphism syndrome	Occurrence	False	Congenital	Inferred relationship	Some	5
Spinocerebellar ataxia dysmorphism syndrome	Occurrence	False	Congenital	Inferred relationship	Some	6
Spinocerebellar ataxia dysmorphism syndrome	Occurrence	False	Congenital	Inferred relationship	Some	7
Spinocerebellar ataxia dysmorphism syndrome	Occurrence	False	Congenital	Inferred relationship	Some	8
Charlie M syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Charlie M syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Charlie M syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	6
Charlie M syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	7
German syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
German syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5

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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)