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
Congenital coronary artery fistula	Occurrence	False	Congenital	Inferred relationship	Some	2
Asymmetric crying face association	Occurrence	False	Congenital	Inferred relationship	Some	2
Klinefelter syndrome, male with 46,XX karyotype (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital absence, atresia and stenosis of small intestine	Occurrence	False	Congenital	Inferred relationship	Some	5
Congenital absence, atresia and stenosis of small intestine	Occurrence	False	Congenital	Inferred relationship	Some	6
Congenital elongation of innominate artery	Occurrence	False	Congenital	Inferred relationship	Some	3
Chromosome 1p36 deletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital deformity of scapula (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Mosaicism 45, X; 46, XX	Occurrence	False	Congenital	Inferred relationship	Some	1
Mosaic XY/XXY	Occurrence	True	Congenital	Inferred relationship	Some	1
22q13.3 deletion syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital abnormal shape of vomer	Occurrence	False	Congenital	Inferred relationship	Some	2
trisomi för hel kromosom, meiotisk icke-disjunktion	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital atresia of artery	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenital complete atrioventricular heart block	Occurrence	True	Congenital	Inferred relationship	Some	1
Trisomy and partial trisomy of autosome	Occurrence	True	Congenital	Inferred relationship	Some	1
21q partial trisomy (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
partiellt trisomi 8p-syndrom	Occurrence	False	Congenital	Inferred relationship	Some	1
4q partial monosomy syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
XY females	Occurrence	True	Congenital	Inferred relationship	Some	1
partiellt trisomi 16p-syndrom	Occurrence	False	Congenital	Inferred relationship	Some	1
medfödd megakolon, icke-aganglionär	Occurrence	False	Congenital	Inferred relationship	Some	2
Triploidy syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital atresia of left main stem coronary artery	Occurrence	True	Congenital	Inferred relationship	Some	1
Anomaly of chromosome pair 18	Occurrence	True	Congenital	Inferred relationship	Some	1
mosaikism 45, X/annan cellinje med avvikande könskromosom	Occurrence	False	Congenital	Inferred relationship	Some	1
Four X syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital arteriovenous fistula occlusion	Occurrence	False	Congenital	Inferred relationship	Some	3
Polyploidy syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
partiellt monosomi 12p-syndrom	Occurrence	False	Congenital	Inferred relationship	Some	1
Anomaly of chromosome pair 1	Occurrence	True	Congenital	Inferred relationship	Some	1
Capillary-venous malformation	Occurrence	False	Congenital	Inferred relationship	Some	4
Klinefelter's syndrome, XXYY (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
22q partial trisomy (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Bilateral incomplete cleft lip and bilateral incomplete cleft of alveolar process of maxilla (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	5
Submucous cleft of hard palate	Occurrence	False	Congenital	Inferred relationship	Some	3
Deletion of short arm of chromosome 18	Occurrence	True	Congenital	Inferred relationship	Some	1
Klinefelters syndrom	Occurrence	False	Congenital	Inferred relationship	Some	1
Central incomplete cleft palate	Occurrence	False	Congenital	Inferred relationship	Some	3
Anomaly of chromosome pair 16	Occurrence	True	Congenital	Inferred relationship	Some	1
Pallister-Killians syndrom	Occurrence	False	Congenital	Inferred relationship	Some	1
medfödd blockering av tårgång	Occurrence	False	Congenital	Inferred relationship	Some	2
Tetrasomy 18p	Occurrence	True	Congenital	Inferred relationship	Some	1
Whole chromosome trisomy syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
5p partial monosomy syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital adhesions of omentum	Occurrence	False	Congenital	Inferred relationship	Some	2
22q partial monosomy (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
1q21.1 microdeletion	Occurrence	True	Congenital	Inferred relationship	Some	1
stavmonokromasi	Occurrence	False	Congenital	Inferred relationship	Some	1
Whole chromosome trisomy meiotic nondisjunction (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital cerebral arteriovenous aneurysm (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
FRAXE	Occurrence	False	Congenital	Inferred relationship	Some	1
18p partial monosomy syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Klinefelter's syndrome, XY/XXY mosaic	Occurrence	False	Congenital	Inferred relationship	Some	1
Trisomy 8	Occurrence	True	Congenital	Inferred relationship	Some	1
Ring chromosome 1 syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Anomaly of sex chromosome	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital enlargement of coronary sinus	Occurrence	True	Congenital	Inferred relationship	Some	1
11q partial monosomy syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital diverticulum of left ventricle	Occurrence	False	Congenital	Inferred relationship	Some	2
Trisomy 12	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital achalasia of esophagus	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital choroidal fold	Occurrence	False	Congenital	Inferred relationship	Some	2
Ring chromosome 14 syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Emanuel syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Fetus with complete trisomy 13 syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Congenital kyphosis	Occurrence	False	Congenital	Inferred relationship	Some	2
Male infertility of developmental origin	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital lacrimal fistula	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenital obstruction of ureteropelvic junction	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenital quadriplegia	Occurrence	True	Congenital	Inferred relationship	Some	1
Lateral meningocele	Occurrence	False	Congenital	Inferred relationship	Some	2
Diffuse smooth muscle hamartoma	Occurrence	False	Congenital	Inferred relationship	Some	3
Gardner syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Port-wine stain in proteus syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
hydromeningocele	Occurrence	False	Congenital	Inferred relationship	Some	4
Congenital His bundle tachycardia	Occurrence	True	Congenital	Inferred relationship	Some	1
Cor triloculare (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	4
Congenital malformation of blood vessel of orbit proper (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenital malformation of blood vessel of orbit proper (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	3
Congenital sacral meningocele	Occurrence	False	Congenital	Inferred relationship	Some	4
Congenital fistula of rectum	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenital fistula of urachus	Occurrence	False	Congenital	Inferred relationship	Some	2
medfött pigmenterat jättenevus i hud	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenitally impaired spermatogenesis	Occurrence	True	Congenital	Inferred relationship	Some	1
Centrofacial lentiginosis syndrome	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenital male infertility	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital pigmented melanocytic nevus (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital rectocloacal fistula	Occurrence	False	Congenital	Inferred relationship	Some	3
Congenital rectocloacal fistula	Occurrence	False	Congenital	Inferred relationship	Some	4
Congenital impairment of spermatozoa motility (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Nodular embryo	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital obstructive azoospermia	Occurrence	True	Congenital	Inferred relationship	Some	1
Cerebral-retinal arteriovenous aneurysm (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
7q partial monosomy	Occurrence	True	Congenital	Inferred relationship	Some	1
cylindriskt embryo	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital dysmotility of small intestine (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
kranialt hydromeningocele	Occurrence	False	Congenital	Inferred relationship	Some	7
Uniatrial biventricular connection with absent right sided atrioventricular connection with straddling valve (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Vertical retraction syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
neurokutan melanos	Occurrence	False	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)