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66091009: Congenital disease (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
109766011 Congenital disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500308011 Congenital disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
805666017 Congenital disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
109766011 Congenital disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
109766011 Congenital disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500308011 Congenital disorder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
500308011 Congenital disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500309015 Congenital abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
500310013 Fetal developmental abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
805666017 Congenital disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
805666017 Congenital disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3011638011 Foetal developmental abnormality en Synonym (core metadata concept) Active Only initial character 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 Switzerland NRC maintained Module
10211000188115 pathologie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3921000077116 maladie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
10211000188115 pathologie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

10200 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital disease Is a Disease false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital disease Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital disease Is a Disorder of foetus and/or newborn true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Talipes (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Occipital meningocele (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Right-sided pulmonary arterial trunk Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital functional disorders of the small intestine Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Vitamin D-dependent rickets, type 2 (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Oto-onycho-peroneal syndrome (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Solitary aortic trunk with pulmonary atresia Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital brain damage (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Spleen in right sided position (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital claw toe (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital peripheral aneurysm Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Vitamin D-dependent rickets, type 1 Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Myostatin related hypertrophy of muscle Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital atrophy of left lobe of liver Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Truncal valve dysplasia Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital vascular disorder Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Tripartite right ventricle Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital conduction defect Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Pericarditis secondary to Mulibrey nanism Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Abnormal root proximity between adjacent teeth Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital disorder of gallbladder and biliary tract Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Posterior deviation of infundibular septum of obstructive aortic arch type (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary valve overriding ventricular septum Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Stomach in right sided position Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Stomach in central position (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Primary endocardial fibroelastosis of left ventricle Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Unipartite right ventricle (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Truncal valve overriding ventricular septum (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital volvulus of stomach Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital contracture of toe joint Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital kyphosis Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Obstructed interchordal space of tricuspid chordae tendinae (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Right inferior caval vein connecting to left atrium and right atrium Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Myelocele Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Prominent valve of inferior vena cava Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hepatomegaly Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Right inferior vena cava connecting to left sided atrium (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Endocardial fibroelastosis of right atrium Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Right atrial appendage - left - juxtaposition Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Supramitral left atrial ring Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Right atrial appendage absent (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
True cleft of common atrioventricular valve leaflet Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Patent foramen ovale Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Spinal hydromeningocele Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Tricuspid valve primary chords absent Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Spinal meningocele Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital positional plagiocephaly Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital renal cyst (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital ischaemic atrophy of central nervous system structure Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Rudimentary left ventricle Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital stenosis Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Right ventricular myocardial sinusoids Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital fecaliths causing obstruction Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital accessory skin tag Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hydrocele Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Preauricular fistula Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pes planus Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital valgus deformity of foot Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nephritis Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Pseudomonas pyocyaneus congenital infection (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Progressive congenital rubella encephalomyelitis Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pancreatic trypsin deficiency (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nephrotic syndrome Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hernia of urinary bladder (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital functional disorders of the colon Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Biotin-thiamine-responsive basal ganglia disease (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Cap myopathy Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital rectal fissure (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Multiple supernumerary teeth unrelated to systemic condition Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital single renal cyst (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Dental midlines coincident and incorrect Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anal fissure (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
perte en longueur de l'arcade dentaire causée par l'absence congénitale de dents Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pulmonary alveolar proteinosis (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital plagiocephaly with pelvic obliquity (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Allantoic cyst Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Redundant prepuce (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hydrosalpinx Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital blepharophimosis of lower eyelid Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital blepharophimosis of upper eyelid Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Longitudinal deficiency of limb Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital skin contracture Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital laryngeal adductor palsy Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital laryngeal abductor palsy Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Ectopic bone tissue, congenital Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Generalized congenital intestinal dysmotility (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital palato-esophageal incoordination Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Arthrogryposis Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital blepharophimosis Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital viral hepatitis (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Angeborenes Glaukom Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pseudostrabismus (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital melanocytic nevus of trunk (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital calcium pyrophosphate dihydrate crystal deposition disease Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital uraemia Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pseudoporencephaly Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic inflammatory corneal disorder characterized by anterior stromal corneal opacification and vascularization of the peripheral cornea with potential central progression and subsequent reduction in visual acuity. Variable features include abnormalities of the iris, such as stromal defects and ectropion uveae, as well as foveal hypoplasia. Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Intestinal epithelial dysplasia Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital amegakaryocytic thrombocytopenia (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital alpha-2-antiplasmin deficiency Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
A rare hemorrhagic disorder due to a constitutional hemostatic factors defect characterized by premature lysis of hemostatic clots and a moderate bleeding tendency. Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)

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