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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
Supernumerary ear lobule Occurrence False Congenital Inferred relationship Existential restriction modifier
Brachymetapody Occurrence False Congenital Inferred relationship Existential restriction modifier
Phosphatidylcholine-sterol acyltransferase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Juvenile type megaloblastic anemia Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Umbilical hernia Occurrence False Congenital Inferred relationship Existential restriction modifier
Immature fetus Occurrence False Congenital Inferred relationship Existential restriction modifier
Diastematomyelia Occurrence False Congenital Inferred relationship Existential restriction modifier 4
Congenital anomaly of retina Occurrence False Congenital Inferred relationship Existential restriction modifier
Non-fluoride enamel opacities Occurrence False Congenital Inferred relationship Existential restriction modifier
Microgyria Occurrence False Congenital Inferred relationship Existential restriction modifier
Ectopic adrenal gland Occurrence False Congenital Inferred relationship Existential restriction modifier
Double ureter Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital atresia of ureter Occurrence False Congenital Inferred relationship Existential restriction modifier
Severe combined immunodeficiency due to absent T cell receptor Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Adult chronic GM2 gangliosidosis Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Congenital anomaly of gallbladder Occurrence False Congenital Inferred relationship Existential restriction modifier
Succinate-semialdehyde dehydrogenase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Bilateral congenital macrostomia Occurrence False Congenital Inferred relationship Existential restriction modifier
Disto-occlusion of teeth Occurrence False Congenital Inferred relationship Existential restriction modifier
Podencephalus Occurrence False Congenital Inferred relationship Existential restriction modifier
Ectopic fetus Occurrence False Congenital Inferred relationship Existential restriction modifier
Familial lipoprotein deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
FG syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Lysinuric protein intolerance, type 1 Occurrence False Congenital Inferred relationship Existential restriction modifier
Osteochondrodysplasia with osteopetrosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Beals auriculo-osteodysplasia syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Kernicterus of newborn Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital enlargement of nasopharynx Occurrence False Congenital Inferred relationship Existential restriction modifier
Funnel-shaped pelvis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital stenosis of aqueduct of Sylvius Occurrence False Congenital Inferred relationship Existential restriction modifier
Complete unilateral cleft palate with cleft lip Occurrence False Congenital Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 9 Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital atresia of bronchus Occurrence False Congenital Inferred relationship Existential restriction modifier
Fordyce's disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Testosterone 17-beta-dehydrogenase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Double Y syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Sinus pericranii Occurrence False Congenital Inferred relationship Existential restriction modifier
Accessory skeletal muscle Occurrence False Congenital Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome, type 8 Occurrence False Congenital Inferred relationship Existential restriction modifier
Brachypellic pelvis Occurrence False Congenital Inferred relationship Existential restriction modifier
Ectopic testis Occurrence False Congenital Inferred relationship Existential restriction modifier
Grob's syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of bronchus Occurrence False Congenital Inferred relationship Existential restriction modifier
Accessory nipple Occurrence False Congenital Inferred relationship Existential restriction modifier
Gangliosidosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital fistula of urachus Occurrence False Congenital Inferred relationship Existential restriction modifier
22q partial trisomy Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital organoaxial volvulus of stomach Occurrence False Congenital Inferred relationship Existential restriction modifier
Leukodystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Agenesis of corpus callosum Occurrence False Congenital Inferred relationship Existential restriction modifier
Erythropoietic protoporphyria Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital obstruction of bile duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Diprosopus tetrophthalmus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital constriction of pylorus Occurrence False Congenital Inferred relationship Existential restriction modifier
Birthmark Occurrence False Congenital Inferred relationship Existential restriction modifier
Transient neonatal hyperglycinemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital atresia of duodenum Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital melanosis of sclera Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Epitheliogenesis imperfecta lingua bovis Occurrence False Congenital Inferred relationship Existential restriction modifier
Bifid thumb Occurrence False Congenital Inferred relationship Existential restriction modifier
Asymmetric crying face association Occurrence False Congenital Inferred relationship Existential restriction modifier
Cranio-orbito-ocular dysraphia syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Acquired pulsion diverticulum of esophagus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital atresia of aortic valve Occurrence False Congenital Inferred relationship Existential restriction modifier
Complete trisomy 18 syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Marginal insertion of umbilical cord Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital laryngocele Occurrence False Congenital Inferred relationship Existential restriction modifier
Ectopic anus Occurrence False Congenital Inferred relationship Existential restriction modifier
Werner syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital malaria Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of all fingers Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of skull Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of prostate Occurrence False Congenital Inferred relationship Existential restriction modifier
Taurodontism Occurrence False Congenital Inferred relationship Existential restriction modifier
Cerebro-costo-mandibular syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital malposition of cardiac apex Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of ureter Occurrence False Congenital Inferred relationship Existential restriction modifier
Disorder of tryptophan metabolism Occurrence False Congenital Inferred relationship Existential restriction modifier
17p partial trisomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Prune belly syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Akabane virus disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Spondyloepiphyseal dysplasia tarda Occurrence False Congenital Inferred relationship Existential restriction modifier
Dysmorphic sialidosis, infantile form Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital bent nose Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of ulna Occurrence False Congenital Inferred relationship Existential restriction modifier
Myxomatosis of cardiac valve Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital human immunodeficiency virus infection Occurrence False Congenital Inferred relationship Existential restriction modifier
Infantile lobar overinflation of lung Occurrence False Congenital Inferred relationship Existential restriction modifier
Enlarged tongue Occurrence False Congenital Inferred relationship Existential restriction modifier
Universal mesentery Occurrence False Congenital Inferred relationship Existential restriction modifier
Niemann-Pick disease, type A Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ocular albinism-lentigines-deafness syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Dysmorphic sialidosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Intermittent branched-chain ketonuria Occurrence False Congenital Inferred relationship Existential restriction modifier
Linear sebaceous nevus sequence Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of coronary artery Occurrence False Congenital Inferred relationship Existential restriction modifier
Homocystinemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Fetal myelomeningocele causing disproportion Occurrence False Congenital Inferred relationship Existential restriction modifier
Meningoencephalocele Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier

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