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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
Infantile cortical hyperostosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Infantile cortical hyperostosis Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Langer mesomelic dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Spina bifida with hydrocephalus of late onset Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Spina bifida with hydrocephalus of late onset Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Preaxial deficiency, postaxial polydactyly, hypospadias syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Preaxial deficiency, postaxial polydactyly, hypospadias syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Preaxial deficiency, postaxial polydactyly, hypospadias syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Spina bifida without hydrocephalus Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Fibrous dysplasia Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Deafness with cataract and skeletal anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Deafness with cataract and skeletal anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Left ventricular outflow tract obstruction due to aneurysm of membranous septum Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with ventricular component under inferior bridging leaflet with chords to crest ventricular septum Occurrence True Congenital Inferred relationship Existential restriction modifier 1
X-linked dominant chondrodysplasia Chassaing Lacombe type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Preaxial polydactyly of toe Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Brachymetapody Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Brachymetapody Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Short stature Brussels type Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Short stature Brussels type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Eiken syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Eiken syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Spondylodysplasia, Torrance type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cystic testicular dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Podencephalus Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Leptocephaly Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital coronary arteriovenous fistula Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Persistent dorsal mesentery Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Ectodermal dysplasia with tooth-nail-sweating defect Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Color changes during tooth formation Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Anomalous pulmonary venous drainage Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Nasal encephalocele Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Left ventricular outflow tract obstruction due to prolapsed arterial valve Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Geographic retinal dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Microcephalus with albinism and digital anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Microcephalus with albinism and digital anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Microcephalus with albinism and digital anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hyperplastic chondrodystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Oculogastrointestinal muscular dystrophy Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Heart-hand syndrome type 3 Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Heart-hand syndrome type 3 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Heart-hand syndrome type 3 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Cervical hemivertebra- balanced Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Disseminated superficial actinic porokeratosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Spondyloenchondromatosis with basal ganglia calcification Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Hypoplasia and coloboma of alar cartilage with telecanthus syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Colloid cyst of third ventricle Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Dyskeratosis congenita Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Bowed tibia, radial anomaly, osteopenia, fracture syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Derencephalus Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Bruck syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Reifenstein syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Congenital arteriovenous fistula hemorrhage Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Grant syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Oculopalatocerebral syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Oculopalatocerebral syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Nemaline myopathy, early onset type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Nasal glial heterotopia Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Nasal glial heterotopia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital anomaly of epiglottis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital contracted pelvis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Subdiaphragmatic total anomalous pulmonary venous return Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital pharyngeal polyp Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Craniosynostosis Boston type Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Membranous ventricular septum defect Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital volvulus Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Double outlet left atrium Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Autosomal recessive aplasia cutis congenita of limb Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cutaneous mastocytosis, short stature, hearing loss syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Cutaneous mastocytosis, short stature, hearing loss syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital intrahepatic portal-systemic shunt Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Scimitar syndrome with additional anomalous pulmonary venous connection Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital bilateral perisylvian syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atresia of larynx and trachea Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Left ventricular outflow tract obstruction due to atrioventricular valve Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Anophthalmos Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Combined deficiency of sialidase AND beta galactosidase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cleft hard palate with left cleft lip Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hyperplasia of islet alpha cells with glucagon excess Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Postaxial polydactyly of toe Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital perforation of the nasal sinus wall Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ophthalmomandibulomelic dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ophthalmomandibulomelic dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Incomplete ossification of nasal bone Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital anterior staphyloma Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Dicephalus dipus tribrachius Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Brachydactyly and distal symphalangism syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Spondylodysplasia, Luton type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Angio-osteohypertrophic syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital abnormality of right atrioventricular valve chordae tendinae in double inlet ventricle Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Fibroblast growth factor receptor 3-related craniosynostosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
X-linked ichthyosis with steryl-sulfatase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Choroidal atrophy and alopecia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Choroidal atrophy and alopecia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2

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