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
Distal limb deficiency with micrognathia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Pachydermoperiostosis of nail	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital hypoplasia of ulna and split foot syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital hypoplasia of ulna and split foot syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital hypoplasia of ulna and split foot syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Embryonic cyst of ovary	Occurrence	True	Congenital	Inferred relationship	Some	1
Dumbbell ossification of centrum of sacral vertebra	Occurrence	True	Congenital	Inferred relationship	Some	1
Hyperphosphatasia-osteoectasia syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Thoracic hemivertebra	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital polyp of ureter	Occurrence	True	Congenital	Inferred relationship	Some	1
Isolation of right common carotid artery (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Ligase 4 syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital bowing of tibia, fibula and femur	Occurrence	True	Congenital	Inferred relationship	Some	1
Familial absence of villi	Occurrence	True	Congenital	Inferred relationship	Some	1
Spina bifida occulta	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital iris ectropion (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Right ventricular outflow tract obstruction due to septoparietal trabeculation (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Incomplete ossification of calcaneus	Occurrence	True	Congenital	Inferred relationship	Some	1
Vomero-premaxillary faciosynostosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Osteogenesis imperfecta, recessive perinatal lethal	Occurrence	True	Congenital	Inferred relationship	Some	1
Ectodermal dysplasia with hair-tooth-nail-sweating defect	Occurrence	True	Congenital	Inferred relationship	Some	1
Epidermolysis bullosa simplex with pyloric atresia	Occurrence	True	Congenital	Inferred relationship	Some	1
Epidermolysis bullosa simplex with pyloric atresia	Occurrence	True	Congenital	Inferred relationship	Some	2
Hirschsprung disease with nail hypoplasia and dysmorphism (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Hirschsprung disease with nail hypoplasia and dysmorphism (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Hirschsprung disease with nail hypoplasia and dysmorphism (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Hirschsprung disease with nail hypoplasia and dysmorphism (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Posteromedial muscle band	Occurrence	True	Congenital	Inferred relationship	Some	1
Omphalocele - irreducible	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital lobar emphysema	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital lobar emphysema	Occurrence	True	Congenital	Inferred relationship	Some	2
Splenoportal vascular anomaly	Occurrence	True	Congenital	Inferred relationship	Some	1
Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Acrocallosal syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Acrocallosal syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Acrodysostosis	Occurrence	True	Congenital	Inferred relationship	Some	3
Aplasia cutis with myopia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital bronchobiliary fistula (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete ossification of squamosal bone	Occurrence	True	Congenital	Inferred relationship	Some	1
medfödda störningar av öga och ögonlocksrörelser	Occurrence	False	Congenital	Inferred relationship	Some	1
Bilateral congenital absence of feet (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital bronchomalacia	Occurrence	True	Congenital	Inferred relationship	Some	1
Kozlowski spondylometaphyseal dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Right ventricular outflow tract obstruction due to aneurysm of membranous septum (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Achondrogenesis, type IA	Occurrence	True	Congenital	Inferred relationship	Some	1
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency	Occurrence	True	Congenital	Inferred relationship	Some	2
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency	Occurrence	True	Congenital	Inferred relationship	Some	1
Ehlers-Danlos syndrome kyphoscoliotic and deafness type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Ehlers-Danlos syndrome kyphoscoliotic and deafness type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Ehlers-Danlos syndrome kyphoscoliotic and deafness type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
X-linked intellectual disability with plagiocephaly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
X-linked intellectual disability with plagiocephaly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Spondyloepiphyseal dysplasia and brachydactyly with speech disorder syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Spondyloepiphyseal dysplasia and brachydactyly with speech disorder syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Thoracic myelocystocele	Occurrence	True	Congenital	Inferred relationship	Some	2
Metaphyseal anadysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Temporo-auro-mandibular dysostosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Generalized dystrophic epidermolysis bullosa	Occurrence	True	Congenital	Inferred relationship	Some	1
MEHMO syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Haim Munk syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Book syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Preductal coarctation of aorta	Occurrence	True	Congenital	Inferred relationship	Some	1
Capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cranial duplication	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital pelvic obliquity (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Noonan syndrome-like disorder with loose anagen hair (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Noonan syndrome-like disorder with loose anagen hair (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Retinal arteriovenous malformation	Occurrence	True	Congenital	Inferred relationship	Some	1
Right ventricular outflow tract obstruction due to malaligned outlet septum (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	1
Hypospadias and intellectual disability syndrome Goldblatt type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
GM1 gangliosidosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete formation of the bony cochlea	Occurrence	True	Congenital	Inferred relationship	Some	1
Arteriovenous malformation of frontonasal process	Occurrence	True	Congenital	Inferred relationship	Some	1
Arteriovenous malformation of frontonasal process	Occurrence	True	Congenital	Inferred relationship	Some	2
Incomplete ossification of interparietal bone	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital uterointestinal fistula	Occurrence	True	Congenital	Inferred relationship	Some	1
Neonatal cutis laxa with marfanoid phenotype	Occurrence	True	Congenital	Inferred relationship	Some	1
Horseshoe kidney	Occurrence	True	Congenital	Inferred relationship	Some	1
McCune Albright syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
McCune Albright syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
McCune Albright syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Trigonocephaly C syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital chordee	Occurrence	True	Congenital	Inferred relationship	Some	1
Bohring Opitz syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Zebra body myopathy	Occurrence	True	Congenital	Inferred relationship	Some	1
Autosomal dominant palmoplantar keratoderma and congenital alopecia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Malrotation of colon and cecum	Occurrence	True	Congenital	Inferred relationship	Some	1
Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Dysosteosclerosis	Occurrence	True	Congenital	Inferred relationship	Some	1

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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)