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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
Splenoportal vascular anomaly Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital abnormality of great veins and coronary sinus Occurrence False Congenital Inferred relationship Existential restriction modifier
Capillary-venous malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Venous-lymphatic malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Capillary-venous-lymphatic malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Bannayan syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Vascular neurocutaneous syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Cavernous hemangiomas of face and supraumbilical midline raphe Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital arteriovenous malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Cerebral arteriovenous malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Parkes Weber syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Truncal arteriovenous fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
Diffuse arteriovenous fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
Hennekam lymphangiectasia-lymphedema syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Arteriovenous angioma Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital arteriovenous fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital arteriovenous fistula occlusion Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital arteriovenous fistula stenosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital arteriovenous fistula thrombosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital arteriovenous fistula infection Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital arteriovenous fistula aneurysm Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital arteriovenous fistula hemorrhage Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital arteriovenous fistula rupture Occurrence False Congenital Inferred relationship Existential restriction modifier
Arteriovenous-lymphatic malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Specific mixed vascular syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Multiple dysplasia syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Weber's true diffuse phlebarteriectasis Occurrence False Congenital Inferred relationship Existential restriction modifier
Familial pulmonary capillary hemangiomatosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Selective malabsorption of cyanocobalamin Occurrence False Congenital Inferred relationship Existential restriction modifier
Muscle phosphofructokinase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Uridine monophosphate hydrolase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Acute intermittent porphyria Occurrence False Congenital Inferred relationship Existential restriction modifier
X-linked agammaglobulinemia with growth hormone deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal agammaglobulinemia with absent B-cells Occurrence False Congenital Inferred relationship Existential restriction modifier
Severe combined immunodeficiency with maternofetal engraftment Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Warts, hypogammaglobulinemia, infections, and myelokathexis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Benign combined immunodeficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Supernumerary cusp Occurrence False Congenital Inferred relationship Existential restriction modifier
Talon cusp Occurrence False Congenital Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type I Occurrence False Congenital Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type II Occurrence False Congenital Inferred relationship Existential restriction modifier
Dentinogenesis imperfecta - Shield's type III Occurrence False Congenital Inferred relationship Existential restriction modifier
Early tooth exfoliation Occurrence False Congenital Inferred relationship Existential restriction modifier
Class II buccal segment relationship - half unit Occurrence False Congenital Inferred relationship Existential restriction modifier
Class III buccal segment relationship - half unit Occurrence False Congenital Inferred relationship Existential restriction modifier
Lateral openbite Occurrence False Congenital Inferred relationship Existential restriction modifier
Lateral openbite - right Occurrence False Congenital Inferred relationship Existential restriction modifier
Lateral openbite - left Occurrence False Congenital Inferred relationship Existential restriction modifier
Traumatic overbite Occurrence False Congenital Inferred relationship Existential restriction modifier
Overbite traumatic to palate Occurrence False Congenital Inferred relationship Existential restriction modifier
Overbite traumatic to labial mucosa Occurrence False Congenital Inferred relationship Existential restriction modifier
Spacing of anterior teeth Occurrence False Congenital Inferred relationship Existential restriction modifier
Impacted tooth Occurrence False Congenital Inferred relationship Existential restriction modifier
Mid-esophageal diverticulum Occurrence False Congenital Inferred relationship Existential restriction modifier
Mid-esophageal pulsion diverticulum Occurrence False Congenital Inferred relationship Existential restriction modifier
Tracheoesophageal fistula without atresia of esophagus Occurrence False Congenital Inferred relationship Existential restriction modifier
Familial absence of villi Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IA Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IIA Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IIB Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IIC Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IIIA Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IIIB Occurrence False Congenital Inferred relationship Existential restriction modifier
Glycogen storage disease type IX Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital disorder of gallbladder and biliary tract Occurrence False Congenital Inferred relationship Existential restriction modifier
Biliary malformation associated with renal tubular insufficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Ichthyosis congenita with biliary atresia Occurrence False Congenital Inferred relationship Existential restriction modifier
Polycystic disease of pancreas Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital malformation of pancreas Occurrence False Congenital Inferred relationship Existential restriction modifier
Cystic fibrosis of pancreas Occurrence False Congenital Inferred relationship Existential restriction modifier
Strangulated umbilical hernia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital umbilical defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Familial mesangial sclerosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital nephrotic syndrome with focal glomerulosclerosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Drash syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Medullary sponge kidney Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital Fanconi syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Acquired Fanconi syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Adult Fanconi syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Dibasic aminoaciduria Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital renal artery aneurysm Occurrence False Congenital Inferred relationship Existential restriction modifier
Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness Occurrence False Congenital Inferred relationship Existential restriction modifier
Ochoa syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Primary vesicoureteric reflux Occurrence False Congenital Inferred relationship Existential restriction modifier
Derodidymis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital familial idiopathic priapism Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital abnormality of scrotum Occurrence False Congenital Inferred relationship Existential restriction modifier
Bifid scrotum Occurrence False Congenital Inferred relationship Existential restriction modifier
Hypogonadism with prune belly syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Variation of umbilical cord Occurrence False Congenital Inferred relationship Existential restriction modifier
Long umbilical cord Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of bone and joint Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hypothyroidism without goiter Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital thyroid hypoplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital atrophy of thyroid Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of mixed type Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital iodine deficiency syndrome of neurological type Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital adrenal hypoplasia, X-linked Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal dominant hypophosphatemic rickets Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal dominant hypophosphatemic bone disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal recessive hypophosphatemic bone disease Occurrence False Congenital Inferred relationship Existential restriction modifier

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