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255399007: Congenital (qualifier value)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
380598010 Congenital en Synonym Active Entire term case insensitive SNOMED CT core module
380599019 Congenita en Synonym Active Entire term case insensitive SNOMED CT core module
646433016 Congenital (qualifier value) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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

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