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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
Malignant melanoma arising in congenital nevus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital lymphangioma Occurrence False Congenital Inferred relationship Existential restriction modifier
Muehrcke's lines Occurrence False Congenital Inferred relationship Existential restriction modifier
Micronychia Occurrence False Congenital Inferred relationship Existential restriction modifier
Persistent urogenital sinus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital thrombocytopenic purpura Occurrence False Congenital Inferred relationship Existential restriction modifier 4
Congenital corneal opacity Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital pulmonary artery aneurysm Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital abnormality of liver and/or biliary tract Occurrence False Congenital Inferred relationship Existential restriction modifier
Indeterminate sex and pseudohermaphroditism Occurrence False Congenital Inferred relationship Existential restriction modifier
Complete congenital duodenal obstruction Occurrence False Congenital Inferred relationship Existential restriction modifier
Neonatal chloridorrhea Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital viral pneumonia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital bacterial pneumonia Occurrence False Congenital Inferred relationship Existential restriction modifier
Intrahepatic biliary hypoplasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Vascular loops of inner ear Occurrence False Congenital Inferred relationship Existential restriction modifier
Vascular malformation of inner ear Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary striate leuconychia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital stricture of common bile duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital abnormality of salivary duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital total lipodystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Manifest-latent nystagmus Occurrence False Congenital Inferred relationship Existential restriction modifier
Placenta increta Occurrence False Congenital Inferred relationship Existential restriction modifier
Duodenal web Occurrence False Congenital Inferred relationship Existential restriction modifier
Progressive congenital rubella encephalomyelitis Occurrence False Congenital Inferred relationship Existential restriction modifier
Hydrocephalus associated with congenital aqueduct stenosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence, atresia and stenosis of large intestine Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital macrocolon, not aganglionic Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital fistula of rectum and anus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital nystagmus with sensory abnormality Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital nystagmus without sensory abnormality Occurrence False Congenital Inferred relationship Existential restriction modifier
Carnitine acetyltransferase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Iatrogenic carnitine deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Hypospadias Occurrence False Congenital Inferred relationship Existential restriction modifier
Posterior keratoconus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital exotropia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital rectocloacal fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
Tyrosinemia type I Occurrence False Congenital Inferred relationship Existential restriction modifier
Hydrencephalomeningocele Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of aortic arch AND/OR descending aorta Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly in number of teeth Occurrence False Congenital Inferred relationship Existential restriction modifier
Total anodontia of permanent dentition Occurrence False Congenital Inferred relationship Existential restriction modifier
Acquired and/or congenital pulmonary valve atresia Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of steroid 11-beta-monooxygenase Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of steroid 17-alpha-monooxygenase Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of steroid 21-monooxygenase Occurrence False Congenital Inferred relationship Existential restriction modifier
Amegakaryocytic thrombocytopenia with congenital malformation Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of hydroxymethylglutaryl-CoA lyase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deficiency of histidine ammonia-lyase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deficiency of methylmalonyl-coenzyme A mutase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
von Willebrand disease, type IIF Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Congenital anomaly of intestinal tract Occurrence False Congenital Inferred relationship Existential restriction modifier
Neonatal disseminated listeriosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 1B Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Encephalomyelitis due to rubella Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital sensory neuropathy with selective loss of small myelinated fibers Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of digestive organ Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of duodenum Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of gastrointestinal tract Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of cornea Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of lens Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of bile duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary von Willebrand disease type 1A Occurrence False Congenital Inferred relationship Existential restriction modifier 2
von Willebrand disease, type 1^a^ Occurrence False Congenital Inferred relationship Existential restriction modifier 2
von Willebrand disease type IA Occurrence False Congenital Inferred relationship Existential restriction modifier 2
von Willebrand disease type 2A Occurrence False Congenital Inferred relationship Existential restriction modifier 2
von Willebrand disease type 2B Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Congenital corneal opacity interfering with vision Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital duplication of stomach Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of lobe of liver Occurrence False Congenital Inferred relationship Existential restriction modifier
Aganglionosis of Auerbach's plexus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital megacolon Occurrence False Congenital Inferred relationship Existential restriction modifier
Aganglionosis of colon Occurrence False Congenital Inferred relationship Existential restriction modifier
Mesonephric cyst Occurrence False Congenital Inferred relationship Existential restriction modifier
Wolffian cyst Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital muscular subaortic stenosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital stenosis of small intestine Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital atresia of jejunum Occurrence False Congenital Inferred relationship Existential restriction modifier
Malrotation of the intestine type IIID Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of large intestine Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of proline dipeptidase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital stricture of bile duct Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital transposition of stomach Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital phlebectasia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital pyloric membrane Occurrence False Congenital Inferred relationship Existential restriction modifier
Placenta previa centralis Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Congenital duodenal stenosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Acquired megaduodenum Occurrence False Congenital Inferred relationship Existential restriction modifier
Autosomal recessive isolated somatotropin deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital duodenal obstruction Occurrence False Congenital Inferred relationship Existential restriction modifier
Microcolon Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital secretory diarrhea, sodium type Occurrence False Congenital Inferred relationship Existential restriction modifier
Ovotestis Occurrence False Congenital Inferred relationship Existential restriction modifier
von Willebrand disease, type IIC Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Ectopic pancreas Occurrence False Congenital Inferred relationship Existential restriction modifier
von Willebrand disease, type IIB Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Congenital myotonia, autosomal recessive form Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital liver grooves Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital postural scoliosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Ambiguous genitalia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital zonular cataract Occurrence False Congenital Inferred relationship Existential restriction modifier

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