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 dysplasia of truncal valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Common atrioventricular valve with unbalanced commitment of valve to ventricle	Occurrence	True	Congenital	Inferred relationship	Some	1
Common atrioventricular valve with unbalanced commitment of valve to right ventricle (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Perimembranous inlet ventricular septal defect (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Syndactyly of toes with fusion of bones of toes of bilateral feet (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Syndactyly of toes with fusion of bones of toes of bilateral feet (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Intermediate atrioventricular septal defect with atrial and ventricular components and separate atrioventricular valves	Occurrence	True	Congenital	Inferred relationship	Some	1
Intermediate atrioventricular septal defect with atrial and ventricular components and separate atrioventricular valves	Occurrence	True	Congenital	Inferred relationship	Some	2
Common atrium with common atrioventricular junction (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Common atrium with common atrioventricular junction (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Atrioventricular septal defect with ventricular imbalance	Occurrence	True	Congenital	Inferred relationship	Some	1
Doubly committed juxta-arterial ventricular septal defect with anteriorly malaligned fibrous outlet septum and muscular postero-inferior rim	Occurrence	True	Congenital	Inferred relationship	Some	1
Doubly committed juxta-arterial ventricular septal defect with anteriorly malaligned fibrous outlet septum and muscular postero-inferior rim	Occurrence	True	Congenital	Inferred relationship	Some	2
Doubly committed juxta-arterial ventricular septal defect with anteriorly malaligned fibrous outlet septum and muscular postero-inferior rim	Occurrence	True	Congenital	Inferred relationship	Some	3
Atrioventricular septal defect with balanced ventricles (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrioventricular septal defect with balanced ventricles (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Common atrium with separate arterioventricular junctions (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Common arterial trunk with pulmonary dominance and aortic coarctation	Occurrence	True	Congenital	Inferred relationship	Some	1
Common arterial trunk with pulmonary dominance and aortic coarctation	Occurrence	True	Congenital	Inferred relationship	Some	2
Common arterial trunk with pulmonary dominance and aortic coarctation	Occurrence	True	Congenital	Inferred relationship	Some	3
Common arterial trunk with pulmonary dominance (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Common arterial trunk with pulmonary dominance (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Perimembranous outlet ventricular septal defect with posteriorly malaligned outlet septum (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital hypoplasia of annulus fibrosus of aorta (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Tricuspid atresia with absent right atrioventricular connection	Occurrence	True	Congenital	Inferred relationship	Some	1
Tricuspid atresia with absent right atrioventricular connection	Occurrence	True	Congenital	Inferred relationship	Some	2
Mitral atresia with imperforate mitral valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Muscular ventricular septal defect opening to right ventricular inlet	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital anomaly of left ventricle (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Double inlet to solitary ventricle of indeterminate morphology (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atypical left ventricular component of common atrioventricular valve (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Disorder of ascending aorta due to conotruncal malformation	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital right ventricular anomaly	Occurrence	True	Congenital	Inferred relationship	Some	1
Atypical right ventricular component of common atrioventricular valve (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital anomaly of left-sided atrioventricular valve in double inlet ventricle (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Perimembranous inlet ventricular septal defect with atrioventricular septal malalignment (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Syndactyly of toes with fusion of bones of toes of bilateral feet (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Syndactyly of toes with fusion of bones of toes of bilateral feet (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Thoracic myelocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Doubly committed juxta-arterial ventricular septal defect with anteriorly malaligned fibrous outlet septum and muscular postero-inferior rim	Occurrence	False	Congenital	Inferred relationship	Some	4
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis	Occurrence	True	Congenital	Inferred relationship	Some	3
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis	Occurrence	True	Congenital	Inferred relationship	Some	2
Right atrial appendage absent	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital absence of chordae tendineae of tricuspid valve (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital absence of carpal bone and metacarpal bone	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital absence of carpal bone and metacarpal bone	Occurrence	True	Congenital	Inferred relationship	Some	2
Aplasia cutis congenita of limb (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Agenesis of tarsal bone and metatarsal bone	Occurrence	True	Congenital	Inferred relationship	Some	1
Agenesis of tarsal bone and metatarsal bone	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital malformation caused by valproic acid	Occurrence	True	Congenital	Inferred relationship	Some	1
Rokitansky sequence	Occurrence	True	Congenital	Inferred relationship	Some	3
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Syndactyly of toes of bilateral feet (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Syndactyly of toes of bilateral feet (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Bilateral megalencephaly	Occurrence	True	Congenital	Inferred relationship	Some	1
Bilateral megalencephaly	Occurrence	True	Congenital	Inferred relationship	Some	2
Alpha-N-acetylgalactosaminidase deficiency type 1	Occurrence	True	Congenital	Inferred relationship	Some	1
14q32 deletion syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
14q32 deletion syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
14q32 deletion syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
Alpha-N-acetylgalactosaminidase deficiency type 2	Occurrence	True	Congenital	Inferred relationship	Some	1
Alpha-N-acetylgalactosaminidase deficiency type 3 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
11p15 deletion syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
11p15 deletion syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
11p15 duplication syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
12q15 deletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
12q15 deletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
12q24.31-q24.32 deletion syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
17q11 deletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
17q11 deletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
17q11 deletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
17q11 deletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
46,XY disorder of sex development	Occurrence	True	Congenital	Inferred relationship	Some	1
46,XX androgen-induced disorder of sex development due to maternal adrenal hyperplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Double orifice of common atrioventricular valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Double orifice of common atrioventricular valve	Occurrence	True	Congenital	Inferred relationship	Some	2
46,XX androgen-induced disorder of sex development of iatrogenic maternal origin	Occurrence	True	Congenital	Inferred relationship	Some	1
46,XX disorder of sex development due to synthetic oral progestogen	Occurrence	True	Congenital	Inferred relationship	Some	1
46,XX disorder of sex development caused by synthetic oral diethylstilbestrol	Occurrence	True	Congenital	Inferred relationship	Some	1
46,XX disorder of sex development caused by testosterone and/or testosterone derivative	Occurrence	True	Congenital	Inferred relationship	Some	1
46,XX testicular disorder of sex development (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atresia of ileum type I	Occurrence	True	Congenital	Inferred relationship	Some	1
Atresia of ileum type II	Occurrence	True	Congenital	Inferred relationship	Some	1
Atresia of ileum type IIIa (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atresia of jejunum type I (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atresia of jejunum type II	Occurrence	True	Congenital	Inferred relationship	Some	1
Atresia of jejunum type IIIa (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
17q23.1-q23.2 duplication syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
17q23.1-q23.2 duplication syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
17q24-qter duplication syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
17q24-qter duplication syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
20p12.2 deletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
20p12.2 deletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
3p25.3 deletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
3p25.3 deletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
5q22.2 deletion syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
5q22.2 deletion syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2

Start Previous Page 306 of 322 Next End

This concept is not in any reference sets

Back to Start

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)