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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
Retroaortic brachiocephalic vein Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Interatrial communication through coronary sinus orifice Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ventricular septal defect with posterior malaligned outlet septum with overriding aortic valve Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ventricular septal defect with anterior malaligned outlet septum with overriding aortic valve Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Total anomalous pulmonary venous connection of supracardiac type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Coarctation of right pulmonary artery Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Total anomalous pulmonary venous connection of intracardiac type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Infracardiac location of anomalous pulmonary venous connection Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Intracardiac location of anomalous pulmonary venous connection Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Double outlet right ventricle with doubly committed ventricular septal defect and pulmonary stenosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Total anomalous pulmonary venous connection of infracardiac type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Coarctation of left pulmonary artery Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Common atrioventricular valve in functionally univentricular heart Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Double outlet right ventricle with subpulmonary ventricular septal defect Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Left inferior vena cava connecting to left sided atrium Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Left inferior vena cava connecting to right sided atrium Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Distal origin of brachiocephalic artery with tracheal compression Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ebstein's anomaly of left atrioventricular valve in functionally univentricular heart Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Ebstein's anomaly of left atrioventricular valve in functionally univentricular heart Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ebstein's anomaly of right atrioventricular valve in functionally univentricular heart Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hypoplasia of pulmonary cusps of absent pulmonary valve type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital syphilitic osteochondritis Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital syphilitic osteochondritis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Desmosterolosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Periodontitis co-occurrent with Ehlers-Danlos syndrome type 4 Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Thrombocytopathy, asplenia and miosis Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Hoyeraal-Hreidarsson syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Infective endarteritis at site of aortopulmonary window Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Anomalous origin of circumflex artery from aortic sinus to right of nonfacing aortic sinus and anomalous origin of left anterior descending coronary artery and right coronary artery from aortic sinus to left of nonfacing aortic sinus Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Anomalous origin of left anterior descending artery from aortic sinus to right of nonfacing aortic sinus and anomalous origin of circumflex artery and right coronary artery from aortic sinus to left of nonfacing aortic sinus Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Anomalous origin of left anterior descending artery and right coronary artery from aortic sinus to right of nonfacing aortic sinus and anomalous origin of circumflex artery from aortic sinus to left of nonfacing aortic sinus Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Fibrous dysplasia of bone with intramuscular myxoma Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Timothy syndrome type 1 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Multiple venous malformation of skin and mucous membrane Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Chromosome 11p11.2 deletion syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Chromosome 11p11.2 deletion syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Diaphragmatic hernia, abnormal face and distal limb anomalies Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Diaphragmatic hernia, abnormal face and distal limb anomalies Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Diaphragmatic hernia, abnormal face and distal limb anomalies Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Arthrogryposis-like syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Microcephaly-capillary malformation syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Anhidrotic ectodermal dysplasia with immune deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 6
Anhidrotic ectodermal dysplasia with immune deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 7
Muscular ventricular septal defect in trabecular septum Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital organoaxial volvulus of stomach Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pancreas divisum Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Synchilia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cleft leaflet of tricuspid valve Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Imperforate hymen Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital pigmented melanocytic nevus of skin of neck Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital pigmented melanocytic nevus of skin of scalp Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Situs inversus abdominalis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital mesenteroaxial volvulus of stomach Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Erythrokeratodermia variabilis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Autosomal recessive dyskeratosis congenita Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Autosomal dominant dyskeratosis congenita Occurrence True Congenital Inferred relationship Existential restriction modifier 2
X-linked dyskeratosis congenita Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Situs inversus thoracis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hereditary elliptocytosis due to abnormal protein 4.1 Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Fibrous dysplasia of jaw Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Duchenne muscular dystrophy Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Angelman syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Neu-Laxova syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Neu-Laxova syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Complete phocomelia of upper limb Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cleft leaflet of mitral valve Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome, familial joint laxity type Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Hereditary elliptocytosis due to beta spectrin defect in self-association Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Marshall-Smith syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Kommerell's diverticulum Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Mucopolysaccharidosis IV-A Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Double outlet right ventricle Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Metaphyseal chondrodysplasia, McKusick type Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Septo-optic dysplasia sequence Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Goldberg Shprintzen megacolon syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 6
Steatocystoma multiplex with natal tooth syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Multiple epiphyseal dysplasia Beighton type Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Haddad syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Ehlers-Danlos syndrome kyphoscoliotic and deafness type Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 9
Deafness, enamel hypoplasia, nail defect syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 6
Dermo-odonto dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Hirschsprung disease with deafness and polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Hirschsprung disease with deafness and polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Hirschsprung disease with type D brachydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Johnson neuroectodermal syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Hirschsprung disease of rectosigmoid region Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Extensive aganglionosis Hirschsprung disease Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Okamoto syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 4
Book syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Revesz syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 11
Autosomal recessive spastic paraplegia type 55 Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 57 Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Schimke immuno-osseous dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Retinohepatoendocrinologic syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Retinohepatoendocrinologic syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 2
X-linked hereditary spastic paraplegia Occurrence False Congenital Inferred relationship Existential restriction modifier 2

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