66091009: Congenital disease (disorder)

SNOMED CT Concept\constatation clinique\Disease\Congenital disease

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital disease	est un(e) (attribut)	Disease	true	Inferred relationship	Some
Congenital disease	survenue (attribut)	congénital	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital vascular disorder (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Tripartite right ventricle (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital conduction defect	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Pericarditis secondary to Mulibrey nanism	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Abnormal root proximity between adjacent teeth	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital disorder of gallbladder and biliary tract	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Posterior deviation of infundibular septum of obstructive aortic arch type (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Pulmonary valve overriding ventricular septum (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Stomach in right sided position (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Stomach in central position (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Primary endocardial fibroelastosis of left ventricle	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Unipartite right ventricle (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Truncal valve overriding ventricular septum (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital volvulus of stomach	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital contracture of toe joint	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital kyphosis	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Obstructed interchordal space of tricuspid chordae tendinae (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Right inferior vena cava connecting to left atrium and right atrium (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Myelocele	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Prominent valve of inferior vena cava	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital hepatomegaly	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Right inferior vena cava connecting to left sided atrium (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Endocardial fibroelastosis of right atrium	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Right atrial appendage - left - juxtaposition	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Supramitral left atrial ring	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Right atrial appendage absent	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
True cleft of common atrioventricular valve leaflet	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
foramen ovale perméable	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Spinal hydromeningocele	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Tricuspid valve primary chords absent (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Spinal meningocele	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital positional plagiocephaly (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital renal cyst (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital ischaemic atrophy of central nervous system structure	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Rudimentary left ventricle	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital stenosis	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Right ventricular myocardial sinusoids (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital fecaliths causing obstruction (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital accessory skin tag	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital hydrocele	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Preauricular fistula	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
pied plat congénital	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital valgus deformity of foot	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital nephritis	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
infection congénitale à Pseudomonas pyocyaneus	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
encéphalomyélite rubéoleuse congénitale progressive	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital pancreatic trypsin deficiency (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital nephrotic syndrome (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital hernia of bladder	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital functional disorders of the colon	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Biotin-thiamine-responsive basal ganglia disease (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Cap myopathy	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital rectal fissure (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Multiple supernumerary teeth unrelated to systemic condition	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital single renal cyst (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Dental midlines coincident and incorrect	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital anal fissure (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
perte en longueur de l'arcade dentaire causée par l'absence congénitale de dents	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital pulmonary alveolar proteinosis (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital plagiocephaly with pelvic obliquity (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Allantoic cyst	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
prépuce redondant	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital hydrosalpinx	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital blepharophimosis of lower eyelid (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital blepharophimosis of upper eyelid	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Longitudinal deficiency of limb	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital skin contracture	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital laryngeal adductor palsy	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital laryngeal abductor palsy	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Ectopic bone tissue, congenital	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Generalized congenital intestinal dysmotility (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital palato-oesophageal incoordination	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Arthrogryposis	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital blepharophimosis	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital viral hepatitis	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital glaucoma (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital pseudostrabismus	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital melanocytic naevus of trunk	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital calcium pyrophosphate dihydrate crystal deposition disease	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital uraemia	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
pseudoporencéphalie congénitale (trouble)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Autosomal dominant keratitis (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital epithelial dysplasia of intestine (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital amegakaryocytic thrombocytopenia (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital alpha-2-antiplasmin deficiency (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital plasminogen activator inhibitor deficiency type 1 (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
déficit congénital en alpha-foetoprotéine	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Combined pituitary hormone deficiency genetic form (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
diarrhée chronique associée à un déficit en glucoamylase	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Longitudinal deficiency of part of limb (disorder)	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
X-linked endothelial dystrophy of cornea (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital analbuminemia (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital hepatic fibrosis	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
macrothrombocytopénie autosomique dominant	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Anaemia following foetal blood loss	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital folate malabsorption anaemia	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital transferrin deficiency	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital deficiency of intrinsic factor	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Biermer's congenital pernicious anaemia	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Autosomal recessive sideroblastic anemia (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital diverticulitis of small intestine (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some

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Id	Description	Lang	Type	Status	Case?	Module
10211000188115	pathologie congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
109766011	Congenital disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3921000077116	maladie congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
500308011	Congenital disorder	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
660561000077119	maladie congénitale (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
805666017	Congenital disease (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core