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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 arteriovenous fistula stenosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Testicular regression syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cranioosteoarthropathy Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Sternum bifidum Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Mietens syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital phlebectasia Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Junctional epidermolysis bullosa Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hypertelorism Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hay-Wells syndrome of ectodermal dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Spondyloepimetaphyseal dysplasia aggrecan type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital rectovaginal fistula Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cutis laxa, x-linked Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Mannosidosis, type I Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with ventricular imbalance consisting of dominant right ventricle and hypoplastic left ventricle Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital tracheoesophageal fistula with esophageal stenosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital tracheoesophageal fistula with esophageal stenosis Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Carpotarsal osteochondromatosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Faciocardiorenal syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Faciocardiorenal syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Auriculoocular anomaly and cleft lip syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Aniridia, renal agenesis, psychomotor retardation syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Precocious osteodysplasty Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Steinfeld syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Arachnoid / ependymal cyst Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Heart-hand syndrome type 2 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Anencephalus and similar anomalies Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Laryngeal cleft type III Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Thymic aplasia or dysplasia with immunodeficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Multiple intracardiac shunts Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Double aortic valve Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cryptophthalmos syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Craniolenticulosutural dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Craniolenticulosutural dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Craniolenticulosutural dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta type IIA Occurrence True Congenital Inferred relationship Existential restriction modifier 1
14q11.2 microdeletion syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
14q11.2 microdeletion syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Microspherophakia with metaphyseal dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Microspherophakia with metaphyseal dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Ulnar dimelia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Right descending aorta Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with ventricular component under superior bridging leaflet without chordal attachment to ventricular septal crest Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Endocardial fibroelastosis of left atrium Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Segmental neurofibromatosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Albinoidism Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Incomplete bilateral cleft palate Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Craniosynostosis with facial dysmorphism and brachydactyly syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Craniosynostosis with facial dysmorphism and brachydactyly syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Craniosynostosis with facial dysmorphism and brachydactyly syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Townes syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex with hypodontia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lissencephaly type 3 metacarpal bone dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Talipomanus Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Mixed sclerosing bone dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cleidocranial dysostosis Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Cleidocranial dysostosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cleidocranial dysostosis Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Cleidocranial dysostosis Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Retrocaval ureter Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Chondrodysplasia punctata Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cataract glaucoma syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
X-linked distal arthrogryposis multiplex congenita Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Nemaline myopathy Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Hydatid cyst of Morgagni - male Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Birthmark Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Incomplete ossification of maxilla Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Sparse hair with short stature and skin anomaly syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Sparse hair with short stature and skin anomaly syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Siegler Brewer Carey syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Spondylodysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Spina bifida with stenosis of aqueduct of Sylvius Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Ectodermal dysplasia with hair-tooth defects Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 4
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Sialic acid storage disease, severe infantile type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Osteopathia striata Occurrence True Congenital Inferred relationship Existential restriction modifier 1
False tendon - heart Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Double cardiac valve orifice Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Netherton's syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital arteriovenous fistula thrombosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Craniopagus Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Retrosternal thyroid gland Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Synophrys Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Crouzon syndrome with acanthosis nigricans Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Crouzon syndrome with acanthosis nigricans Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Cataract, congenital heart disease, neural tube defect syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Cataract, congenital heart disease, neural tube defect syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cataract, congenital heart disease, neural tube defect syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Cataract, congenital heart disease, neural tube defect syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Multiple epiphyseal dysplasia Beighton type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Odontomicronychial ectodermal dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cherubism with gingival fibromatosis Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Dolichocolon Occurrence True Congenital Inferred relationship Existential restriction modifier 1

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