255399007: Congenital (qualifier value)

SNOMED CT Concept\Qualifier value\...

\Precondition value (qualifier value)\Periods of life\Congenital

\Special atomic mapping values\Special disorder atoms\Temporal periods\Periods of life\Congenital

\Descriptor (qualifier value)\Time patterns\Temporal periods\Periods of life\Congenital

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital	Is a	Periods of life	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Malignant melanoma arising in congenital nevus	Occurrence	False	Congenital	Inferred relationship	Some
Congenital lymphangioma	Occurrence	False	Congenital	Inferred relationship	Some
Muehrcke's lines	Occurrence	False	Congenital	Inferred relationship	Some
Micronychia	Occurrence	False	Congenital	Inferred relationship	Some
Persistent urogenital sinus	Occurrence	False	Congenital	Inferred relationship	Some
kongenital trombocytopen purpura	Occurrence	False	Congenital	Inferred relationship	Some	4
Congenital corneal opacity	Occurrence	False	Congenital	Inferred relationship	Some
Congenital pulmonary artery aneurysm	Occurrence	False	Congenital	Inferred relationship	Some
Congenital abnormality of liver and/or biliary tract (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
obestämbart kön och pseudohermafroditism	Occurrence	False	Congenital	Inferred relationship	Some
Complete congenital duodenal obstruction	Occurrence	False	Congenital	Inferred relationship	Some
neonatal kloridorré	Occurrence	False	Congenital	Inferred relationship	Some
Congenital viral pneumonia	Occurrence	False	Congenital	Inferred relationship	Some
Congenital bacterial pneumonia	Occurrence	False	Congenital	Inferred relationship	Some
Intrahepatic biliary hypoplasia	Occurrence	False	Congenital	Inferred relationship	Some
Vascular loops of inner ear	Occurrence	False	Congenital	Inferred relationship	Some
Vascular malformation of inner ear	Occurrence	False	Congenital	Inferred relationship	Some
Hereditary striate leuconychia (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Congenital stricture of common bile duct	Occurrence	False	Congenital	Inferred relationship	Some
Congenital abnormality of salivary duct	Occurrence	False	Congenital	Inferred relationship	Some
Congenital total lipodystrophy (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Manifest-latent nystagmus	Occurrence	False	Congenital	Inferred relationship	Some
Placenta increta	Occurrence	False	Congenital	Inferred relationship	Some
Duodenal web	Occurrence	False	Congenital	Inferred relationship	Some
Progressive congenital rubella encephalomyelitis	Occurrence	False	Congenital	Inferred relationship	Some
Hydrocephalus associated with congenital aqueduct stenosis (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
medfödd avsaknad, atresi och stenos av tjocktarm	Occurrence	False	Congenital	Inferred relationship	Some
medfödd megakolon, icke-aganglionär	Occurrence	False	Congenital	Inferred relationship	Some
Congenital fistula of rectum and anus	Occurrence	False	Congenital	Inferred relationship	Some
Congenital nystagmus with sensory abnormality	Occurrence	False	Congenital	Inferred relationship	Some
Congenital nystagmus without sensory abnormality	Occurrence	False	Congenital	Inferred relationship	Some
brist på karnitinacetyltransferas	Occurrence	False	Congenital	Inferred relationship	Some
Iatrogenic carnitine deficiency (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Hypospadias	Occurrence	False	Congenital	Inferred relationship	Some
Posterior keratoconus	Occurrence	False	Congenital	Inferred relationship	Some
Congenital exotropia	Occurrence	False	Congenital	Inferred relationship	Some
Congenital rectocloacal fistula	Occurrence	False	Congenital	Inferred relationship	Some
Tyrosinemia type I (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
hydrencefalomeningocele	Occurrence	False	Congenital	Inferred relationship	Some
Congenital anomaly of aortic arch AND/OR descending aorta (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Congenital anomaly in number of teeth (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
total anodonti av permanenta dentitionen	Occurrence	False	Congenital	Inferred relationship	Some
förvärvad och/eller medfödd pulmonalklaffatresi	Occurrence	False	Congenital	Inferred relationship	Some
Deficiency of steroid 11-beta-monooxygenase	Occurrence	False	Congenital	Inferred relationship	Some
Deficiency of steroid 17-alpha-monooxygenase	Occurrence	False	Congenital	Inferred relationship	Some
Deficiency of steroid 21-monooxygenase	Occurrence	False	Congenital	Inferred relationship	Some
Amegakaryocytic thrombocytopenia with congenital malformation	Occurrence	False	Congenital	Inferred relationship	Some
Deficiency of hydroxymethylglutaryl-CoA lyase	Occurrence	True	Congenital	Inferred relationship	Some	1
Deficiency of histidine ammonia-lyase	Occurrence	True	Congenital	Inferred relationship	Some	1
Deficiency of methylmalonyl-coenzyme A mutase (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
von Willebrands sjukdom, typ 2F	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenital anomaly of intestinal tract	Occurrence	False	Congenital	Inferred relationship	Some
Neonatal disseminated listeriosis	Occurrence	False	Congenital	Inferred relationship	Some
Hereditary von Willebrand disease type 1B	Occurrence	False	Congenital	Inferred relationship	Some	2
Encephalomyelitis due to rubella (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Congenital sensory neuropathy with selective loss of small myelinated fibres	Occurrence	False	Congenital	Inferred relationship	Some
Congenital anomaly of digestive organ	Occurrence	False	Congenital	Inferred relationship	Some
Congenital anomaly of duodenum	Occurrence	False	Congenital	Inferred relationship	Some
Congenital anomaly of gastrointestinal tract	Occurrence	False	Congenital	Inferred relationship	Some
Congenital anomaly of cornea	Occurrence	False	Congenital	Inferred relationship	Some
Congenital anomaly of lens (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Congenital absence of bile duct (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Hereditary von Willebrand disease type 1A	Occurrence	False	Congenital	Inferred relationship	Some	2
von Willebrands sjukdom, typ 1a	Occurrence	False	Congenital	Inferred relationship	Some	2
von Willebrands sjukdom, typ 1A	Occurrence	False	Congenital	Inferred relationship	Some	2
von Willebrands sjukdom, typ 2A	Occurrence	False	Congenital	Inferred relationship	Some	2
von Willebrands sjukdom, typ 2B	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenital corneal opacity interfering with vision	Occurrence	False	Congenital	Inferred relationship	Some
Congenital duplication of stomach	Occurrence	False	Congenital	Inferred relationship	Some
Congenital absence of lobe of liver	Occurrence	False	Congenital	Inferred relationship	Some
Aganglionosis of Auerbach's plexus (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
medfödd megakolon	Occurrence	False	Congenital	Inferred relationship	Some
Aganglionosis of colon	Occurrence	False	Congenital	Inferred relationship	Some
Mesonephric cyst	Occurrence	False	Congenital	Inferred relationship	Some
Wolffian cyst	Occurrence	False	Congenital	Inferred relationship	Some
Congenital muscular subaortic stenosis	Occurrence	False	Congenital	Inferred relationship	Some
Congenital stenosis of small intestine	Occurrence	False	Congenital	Inferred relationship	Some
Congenital atresia of jejunum	Occurrence	False	Congenital	Inferred relationship	Some
Malrotation of the intestine type IIID (disorder)	Occurrence	False	Congenital	Inferred relationship	Some
Congenital anomaly of large intestine	Occurrence	False	Congenital	Inferred relationship	Some
Deficiency of proline dipeptidase	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital stricture of bile duct	Occurrence	False	Congenital	Inferred relationship	Some
Congenital transposition of stomach	Occurrence	False	Congenital	Inferred relationship	Some
Congenital phlebectasia	Occurrence	False	Congenital	Inferred relationship	Some
Congenital pyloric membrane	Occurrence	False	Congenital	Inferred relationship	Some
Placenta previa centralis	Occurrence	False	Congenital	Inferred relationship	Some	3
Congenital duodenal stenosis	Occurrence	False	Congenital	Inferred relationship	Some
Acquired megaduodenum	Occurrence	False	Congenital	Inferred relationship	Some
Autosomal recessive isolated somatotropin deficiency	Occurrence	False	Congenital	Inferred relationship	Some
Congenital duodenal obstruction	Occurrence	False	Congenital	Inferred relationship	Some
Microcolon	Occurrence	False	Congenital	Inferred relationship	Some
Congenital secretory diarrhea, sodium type	Occurrence	False	Congenital	Inferred relationship	Some
ovotestis	Occurrence	False	Congenital	Inferred relationship	Some
von Willebrands sjukdom, typ 2C	Occurrence	False	Congenital	Inferred relationship	Some	2
Ectopic pancreas	Occurrence	False	Congenital	Inferred relationship	Some
von Willebrands sjukdom, typ 2B	Occurrence	False	Congenital	Inferred relationship	Some	2
Congenital myotonia, autosomal recessive form	Occurrence	False	Congenital	Inferred relationship	Some
Congenital liver grooves	Occurrence	False	Congenital	Inferred relationship	Some
Congenital postural scoliosis	Occurrence	False	Congenital	Inferred relationship	Some
Ambiguous genitalia	Occurrence	False	Congenital	Inferred relationship	Some
Congenital zonular cataract	Occurrence	False	Congenital	Inferred relationship	Some

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Id	Description	Lang	Type	Status	Case?	Module
380598010	Congenital	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
380599019	Congenita	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
646433016	Congenital (qualifier value)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
135131000052119	medfödd	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)