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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
Congenital absence of bladder and urethra Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Partial anomalous pulmonary venous connection of part of right lung Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Bipartite ossification of supraoccipital bone Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Prune belly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with restrictive ventricular component Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Brachymorphism with onychodysplasia and dysphalangism syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Brachymorphism with onychodysplasia and dysphalangism syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Common arterial trunk with obstruction of aortic arch Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Achondrogenesis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Worth disease Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Aortico-left ventricular tunnel with intracardiac aneurysm of septal portion Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Anodontia of primary dentition Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Polyostotic fibrous dysplasia of bone Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 1 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Penoscrotal hypospadias Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Partial anomalous pulmonary venous connection of part of left lung Occurrence True Congenital Inferred relationship Existential restriction modifier 1
X-linked retinal dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Idiopathic multicentric osteolysis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atresia and stenosis of aorta Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ullrich congenital muscular dystrophy Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ectodermal dysplasia with hair-tooth-nail defects Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Nievergelt's syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cardiocranial syndrome Pfeiffer type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Bilateral muscular infundibula Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Aortico-left ventricular tunnel of simple type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cervical hemivertebra Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cerebellar ataxia co-occurrent with ectodermal dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ectodermal dysplasia and sensorineural deafness syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Ectodermal dysplasia and sensorineural deafness syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Frontonasal dysplasia sequence Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Osteoporosis and macrocephaly with blindness and joint hypermobility syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Osteoporosis and macrocephaly with blindness and joint hypermobility syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Right superior vena cava connecting to coronary sinus Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Right superior vena cava connecting to coronary sinus Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Arteriovenous malformation of face Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Carpenter Waziri syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Congenital partial portal-systemic shunt Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Melorheostosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Melorheostosis Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Cutaneous lesion resulting from spinal dysraphism Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Hall Riggs syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hall Riggs syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Hall Riggs syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Venous remnant Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Incomplete ossification of zygomatic bone Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Microtia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital degeneration of nervous system Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta, dominant perinatal lethal Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Wolcott-Rallison dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ectodermal dysplasia with sweating defect Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital urethrovaginal fistula Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital transverse mandibular hypoplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Trichothiodystrophy Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Trichothiodystrophy Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Sacral spina bifida without hydrocephalus - open Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital eventration of right crus of diaphragm Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital anomaly of fetus Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Mannosidosis, type II Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ameloonychohypohidrotic syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Straddling tricuspid valve Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Agenesis of left kidney co-occurrent with congenital dysplasia of right kidney Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Maxillary dysostosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cicatricial junctional epidermolysis bullosa Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Café-au-lait macules with temporal dysrhythmia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Phocomelia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Metaphyseal chondrodysplasia, Sedaghatian type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Double inlet ventricle Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Desbuquois syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Isolation of branch of aortic arch Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Dermatoosteolysis Kirghizian type Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Dermatoosteolysis Kirghizian type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Salamon's syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Camptodactyly with joint contracture and facial skeletal defect syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Camptodactyly with joint contracture and facial skeletal defect syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Camptodactyly with joint contracture and facial skeletal defect syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pelviscapular dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Right ventricular outflow tract obstruction due to septal hypertrophy Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Partial anomalous pulmonary venous connection with anomalous veins connecting first to pulmonary venous confluence Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Genochondromatosis type 2 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Microcornea with glaucoma and absent frontal sinus syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Short rib dysplasia group (with or without polydactyly) Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Brachytelephalangy, facial dysmorphism, Kallmann syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Gnathodiaphyseal dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1

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