255399007: Congenital (qualifier value)

SNOMED CT Concept\Qualifier value\...

\Precondition value (qualifier value)\Periods of life\Congenital

\Special atomic mapping values\Special disorder atoms\Temporal periods\Periods of life\Congenital

\Descriptor (qualifier value)\Time patterns\Temporal periods\Periods of life\Congenital

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital	Is a	Periods of life	true	Inferred relationship	Some

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

Start Previous Page 278 of 330 Next End

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
380598010	Congenital	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
380599019	Congenita	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
646433016	Congenital (qualifier value)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
135131000052119	medfödd	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)