255399007: Congenital (qualifier value)

SNOMED CT Concept\valeur de l'attribut\...

\Precondition value (qualifier value)\périodes de vie\congénital

\valeurs d'attributs spéciaux\éléments particuliers d'un trouble\périodes temporelles\périodes de vie\congénital

\descripteur\caractéristiques temporelles\périodes temporelles\périodes de vie\congénital

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
congénital	est un(e) (attribut)	périodes de vie	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
[X]Late congenital syphilis, unspecified	survenue (attribut)	False	congénital	Inferred relationship	Some
[X]Congenital syphilis, unspecified	survenue (attribut)	False	congénital	Inferred relationship	Some
infection congénitale à Pseudomonas pyocyaneus	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Keutel syndrome (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	1
chondrodystrophie malacique	survenue (attribut)	False	congénital	Inferred relationship	Some	1
chondrodystrophie malacique	survenue (attribut)	False	congénital	Inferred relationship	Some	2
Hypoplastic chondrodystrophy	survenue (attribut)	True	congénital	Inferred relationship	Some	1
hydarthrose de Clutton	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Hyperplastic chondrodystrophy	survenue (attribut)	False	congénital	Inferred relationship	Some	1
Keutel syndrome (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	4
polyneuropathie syphilitique congénitale tardive	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Other specified congenital hypothyroidism	survenue (attribut)	False	congénital	Inferred relationship	Some
Amino acid transport disorder NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Disturbance of aromatic amino acid metabolism NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Other specified disturbance of branched chain amino acid metabolism (disorder)	survenue (attribut)	False	congénital	Inferred relationship	Some
Disturbance of branched chain amino acid metabolism NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Other specified disturbance of sulfur-bearing amino acid metabolism	survenue (attribut)	False	congénital	Inferred relationship	Some
Other specified disturbance of histidine metabolism	survenue (attribut)	False	congénital	Inferred relationship	Some
Disturbance of histidine metabolism NOS (disorder)	survenue (attribut)	False	congénital	Inferred relationship	Some
Other specified disturbance of urea cycle metabolism (disorder)	survenue (attribut)	False	congénital	Inferred relationship	Some
Disturbance of urea cycle metabolism NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Disturbance of other straight chain amino acid metabolism	survenue (attribut)	False	congénital	Inferred relationship	Some
Disturbance of other straight chain amino acid metabolism NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Disturbance of other specified amino acid metabolism	survenue (attribut)	False	congénital	Inferred relationship	Some
Disturbance of other specified amino acid metabolism NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Disturbance of amino acid transport or metabolism NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Other specified glycogenosis (disorder)	survenue (attribut)	False	congénital	Inferred relationship	Some
Glycogenosis NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Oxaluria NEC	survenue (attribut)	False	congénital	Inferred relationship	Some
Other specified pure hypercholesterolemia	survenue (attribut)	False	congénital	Inferred relationship	Some
Pure hypercholesterolemia NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Hyperlipidemia NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Lipoprotein deficiency NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Other disorders of lipoid metabolism	survenue (attribut)	False	congénital	Inferred relationship	Some
Other disorder of lipoid metabolism NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Disorder of lipoid metabolism NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Gout NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Porphyria NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Other disorder of purine or pyrimidine metabolism NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Other specified congenital hyperbilirubinemia	survenue (attribut)	False	congénital	Inferred relationship	Some
Congenital hyperbilirubinemia NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Other specified mucopolysaccharidosis	survenue (attribut)	False	congénital	Inferred relationship	Some
Mucopolysaccharidosis NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Combined immunity deficiency NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Syringomyelia or syringobulbia NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Congenital hypertrophic pyloric stenosis (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	1
syndrome de microdélétion 14q22q23	survenue (attribut)	True	congénital	Inferred relationship	Some	3
syndrome de microdélétion 14q22q23	survenue (attribut)	True	congénital	Inferred relationship	Some	2
syndrome de microdélétion 14q22q23	survenue (attribut)	True	congénital	Inferred relationship	Some	1
syndrome de microdélétion 14q22q23	survenue (attribut)	True	congénital	Inferred relationship	Some	4
Ogden syndrome (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Mottled tooth NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Micrognathism unspecified	survenue (attribut)	False	congénital	Inferred relationship	Some
Prognathism NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Retrognathism NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Crossbite unspecified (disorder)	survenue (attribut)	False	congénital	Inferred relationship	Some
Open-bite unspecified	survenue (attribut)	False	congénital	Inferred relationship	Some
Tooth crowding NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Abnormal tooth spacing NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Impacted and buried teeth NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Tooth position anomaly NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Solitary arterial trunk	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Keutel syndrome (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	2
syndrome de Jawad	survenue (attribut)	False	congénital	Inferred relationship	Some	2
syndrome de Jawad	survenue (attribut)	False	congénital	Inferred relationship	Some	3
syndrome de Jawad	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Acquired esophageal diverticulum NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Keutel syndrome (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	3
Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Papular epidermal naevi with skyline basal cell layers syndrome	survenue (attribut)	True	congénital	Inferred relationship	Some	2
Papular epidermal naevi with skyline basal cell layers syndrome	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder)	survenue (attribut)	False	congénital	Inferred relationship	Some	4
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	2
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	3
Severe combined immunodeficiency due to CARD11 deficiency	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Autism spectrum disorder due to AUTS2 deficiency	survenue (attribut)	True	congénital	Inferred relationship	Some	1
15q overgrowth syndrome	survenue (attribut)	True	congénital	Inferred relationship	Some	4
15q overgrowth syndrome	survenue (attribut)	True	congénital	Inferred relationship	Some	1
15q overgrowth syndrome	survenue (attribut)	True	congénital	Inferred relationship	Some	3
15q overgrowth syndrome	survenue (attribut)	True	congénital	Inferred relationship	Some	2
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Thrombocythemia with distal limb defect (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	3
Umbilical hernia with gangrene NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Umbilical hernia with obstruction NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Umbilical hernia - irreducible and NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Simple umbilical hernia NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Unspecified umbilical hernia	survenue (attribut)	False	congénital	Inferred relationship	Some
Unspecified omphalocele	survenue (attribut)	False	congénital	Inferred relationship	Some
Facial dysmorphism, immunodeficiency, livedo, short stature syndrome	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Facial dysmorphism, immunodeficiency, livedo, short stature syndrome	survenue (attribut)	True	congénital	Inferred relationship	Some	2
Unspecified paraumbilical hernia	survenue (attribut)	False	congénital	Inferred relationship	Some
Unspecified umbilical hernia NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Umbilical hernia NOS	survenue (attribut)	False	congénital	Inferred relationship	Some
Brachyolmia	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Trichodental syndrome	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Left renal agenesis co-occurrent with right renal hypoplasia	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Generalized junctional epidermolysis bullosa	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Extralobar bronchopulmonary sequestration	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Trigonocephaly with broad thumb syndrome (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	1
Trigonocephaly with broad thumb syndrome (disorder)	survenue (attribut)	True	congénital	Inferred relationship	Some	4

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Id	Description	Lang	Type	Status	Case?	Module
273731000077117	congénital	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
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
554801000077113	congénital (valeur de l'attribut)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
646433016	Congenital (qualifier value)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core