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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
Lutembacher's syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Persistent ostium secundum Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Bronchopulmonary collateral artery Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cerebral-retinal arteriovenous aneurysm Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Hypoplasia of left ventricular inflow tract Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital nonprogressive myopathy with Moebius and Robin sequences Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Palmoplantar keratoderma with clinodactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Palmoplantar keratoderma with clinodactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Incomplete ossification of presphenoid bone Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Interrupted left inferior vena cava Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta type IV Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Schimke immuno-osseous dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Temporal encephalocele Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Eccentric opening of aortic valve Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Left ventricular outflow tract obstruction due to fibromuscular tunnel Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Ramos Arroyo syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Incomplete ossification of basioccipital bone Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Left inferior vena cava connecting to left atrium and right atrium Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lethal autosomal recessive epidermolysis bullosa simplex Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Karsch Neugebauer syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Karsch Neugebauer syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Diastrophic dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Multiple epiphyseal dysplasia tarda type IIIa Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Anonychia with microcephaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Autosomal dominant hypophosphatemic rickets Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Female infertility due to structural congenital anomaly of cervix Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Native American myopathy Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Common truncus arteriosus Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Trisomy 10p Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Trisomy 10p Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Upper limb defect with eye and ear abnormalities syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Right ventricular outflow tract obstruction due to abnormal cardiac muscle bands Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Eccentric opening of tricuspid aortic valve Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Mesomelic dysplasia Savarirayan type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Short stature, pituitary and cerebellar defect and small sella turcica syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Nemaline myopathy, late onset type Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Menkes kinky-hair syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Acrofacial dysostosis Palagonia type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Eichsfeld type congenital muscular dystrophy Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Aniridia type 2 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
FG syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lumbar hemivertebra - unbalanced Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital anourethral fistula Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital pyloric antral membrane Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Right ventricular outflow tract abnormality Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Simple ureterocele Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Doubling of uterus with doubling of cervix and vagina Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Double renal pelvis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Developmental ovarian cyst Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta, type IV A Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Mesomelic dysplasia of hypoplastic ulna and fibula type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Chondrodysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Persistent tunica vasculosa lentis Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Persistent tunica vasculosa lentis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex due to plakophilin deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Epidermolysis simplex superficialis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Dubin-Johnson syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Nodular renal blastema Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Matthew Wood syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital pulmonary lymphangiectasis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Abnormal connection of hepatic vein to atrium Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Enamel spur Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Total congenital alopecia Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Atelosteogenesis type 1 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Winchester syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Frontoethmoidal encephalocele Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hutchinson's triad Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Hereditary neurocutaneous angiomata Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Distal penile hypospadias Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Fibular dimelia diplopodia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Renal dysplasia with limb defect syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Renal dysplasia with limb defect syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital bilateral internal tibial torsion Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital bilateral internal tibial torsion Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Spondyloepiphyseal dysplasia tarda Kohn type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cleft hard and soft palate with right cleft lip Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Cleft hard and soft palate with right cleft lip Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Endosteal hyperostoses with cerebellar hypoplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Left ventricular outflow tract obstruction due to malaligned outlet septum Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Right ventricular muscular infundibular stenosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Completely unroofed coronary sinus defect in left atrium Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Junctional epidermolysis bullosa non-Herlitz type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deaf blind hypopigmentation syndrome Yemenite type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deaf blind hypopigmentation syndrome Yemenite type Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Atelosteogenesis/diastrophic dysplasia Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Rhizomelic chondrodysplasia punctata syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Rhizomelic chondrodysplasia punctata syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Preductal hypoplasia of aorta Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Brain malformation, congenital heart disease, postaxial polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Brain malformation, congenital heart disease, postaxial polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Brain malformation, congenital heart disease, postaxial polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ectodermal dysplasia with hair-nail defect Occurrence True Congenital Inferred relationship Existential restriction modifier 1

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