FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.7  |  FHIR Version n/a  User: [n/a]

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
Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Systemic to pulmonary collateral artery from coronary artery Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Systemic to pulmonary collateral artery from coronary artery Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Familial caudal dysgenesis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Absent ductus venosus Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Dandy-Walker malformation with postaxial polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Dandy-Walker malformation with postaxial polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Dandy-Walker malformation with postaxial polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Bilateral congenital absence of ovary Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Localized dystrophic epidermolysis bullosa Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital hydrocephalus caused by toxoplasmosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa pruriginosa Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Immature ganglionosis of large intestine Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital coronary artery fistula to left ventricle Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Double ureter Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Long thumb brachydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Long thumb brachydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Long thumb brachydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital club finger Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital generalized alopecia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lower moiety ureter of duplex kidney Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Vascular ring with right aortic arch and right patent arterial duct with absent left pulmonary artery Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Persistent pupillary membranes Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Macrodontia Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Right ventricular outflow tract obstruction due to atrioventricular valve Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Neurofibromatosis syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital complete fusion of spine Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Synotus Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Right ventricular outflow obstruction - tubular Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Solitary aortic trunk with pulmonary atresia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pili torti Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Dumbbell ossification of centrum of lumbar vertebra Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Incomplete ossification of basisphenoid bone Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Segmental uterine aplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hypochondroplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cystic leukoencephalopathy without megalencephaly Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital athetosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Opsismodysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Muscular ventricular septal defect in apical trabecular septum Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Meacham syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Meacham syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Marfanoid habitus with autosomal recessive intellectual disability syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
X-linked dominant chondrodysplasia punctata of Happle Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Nasopharyngeal encephalocele Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Chromosome Xq28 trisomy Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Sturge-Weber syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Sturge-Weber syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Acral self-healing collodion baby Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Aphalangy and syndactyly with microcephaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Aphalangy and syndactyly with microcephaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Genetic disorder of surfactant dysfunction Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Partial hypoplasia of optic disc Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cataract with aberrant oral frenula and growth delay syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Incomplete ossification of scapula Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deafness and intellectual disability Martin Probst type syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with ventricular component and shunting under connecting tongue with separate orifices Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome cardiac valvular type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome cardiac valvular type Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital stricture of rectum with fistula Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital malformation of uterus and cervix Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital bent nose Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cervical myelocystocele Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Aortic left ventricular tunnel Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Localized recessive dystrophic epidermolysis bullosa Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex with circinate migratory erythema Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pyle metaphyseal dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital hypoganglionosis of large intestine Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital hypoganglionosis of large intestine Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Trisomy 17p Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Bilateral complete cleft palate with cleft lip Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Bilateral complete cleft palate with cleft lip Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Developmental malformation, deafness, dystonia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital lateral curvature of penis Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Congenital vascular anomaly of eyelid Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal radioulnar synostosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Right ventricular outflow tract obstruction due to fibromuscular shelf Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Atresia of pulmonary trunk with absent left pulmonary artery Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ulceration of umbilical cord and atresia of intestine syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Bilateral congenital primary hydronephrosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Schoepf-Schulz-Passage syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital fistulae between uterus and digestive and urinary tracts Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital fistulae between uterus and digestive and urinary tracts Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Ballard syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deafness craniofacial syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Inherited cutis laxa Occurrence True Congenital Inferred relationship Existential restriction modifier 1
I-cell disease Occurrence True Congenital Inferred relationship Existential restriction modifier 1
X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Coronary artery arising from main pulmonary artery Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Type IV short rib polydactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Distal limb deficiency with micrognathia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Distal limb deficiency with micrognathia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Distal limb deficiency with micrognathia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3

Start Previous Page 278 of 343 Next End

This concept is not in any reference sets

Back to Start