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
Congenital arteriovenous fistula stenosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Testicular regression syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Cranioosteoarthropathy (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Sternum bifidum	Occurrence	True	Congenital	Inferred relationship	Some	1
Mietens syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital phlebectasia	Occurrence	False	Congenital	Inferred relationship	Some	1
Junctional epidermolysis bullosa (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypertelorism	Occurrence	True	Congenital	Inferred relationship	Some	1
Hay-Wells syndrome of ectodermal dysplasia	Occurrence	True	Congenital	Inferred relationship	Some	3
Spondyloepimetaphyseal dysplasia aggrecan type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital rectovaginal fistula	Occurrence	True	Congenital	Inferred relationship	Some	1
Cutis laxa, x-linked	Occurrence	True	Congenital	Inferred relationship	Some	1
Mannosidosis, type I	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrioventricular septal defect with ventricular imbalance consisting of dominant right ventricle and hypoplastic left ventricle (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital tracheoesophageal fistula with esophageal stenosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital tracheoesophageal fistula with esophageal stenosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Carpotarsal osteochondromatosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Faciocardiorenal syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Faciocardiorenal syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
syndrom med aurikulookulär anomali och läppspalt	Occurrence	False	Congenital	Inferred relationship	Some	2
Aniridia, renal agenesis, psychomotor retardation syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Precocious osteodysplasty (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Steinfeld syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
araknoidal eller ependymal cysta	Occurrence	False	Congenital	Inferred relationship	Some	1
Heart-hand syndrome type 2 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
anencefali och liknande missbildningar	Occurrence	False	Congenital	Inferred relationship	Some	1
Laryngeal cleft type III	Occurrence	True	Congenital	Inferred relationship	Some	1
Thymic aplasia or dysplasia with immunodeficiency	Occurrence	True	Congenital	Inferred relationship	Some	1
Multiple intracardiac shunts	Occurrence	True	Congenital	Inferred relationship	Some	1
Double aortic valve	Occurrence	True	Congenital	Inferred relationship	Some	1
Cryptophthalmos syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Craniolenticulosutural dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Craniolenticulosutural dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Craniolenticulosutural dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Osteogenesis imperfecta type IIA	Occurrence	True	Congenital	Inferred relationship	Some	1
14q11.2 microdeletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
14q11.2 microdeletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Microspherophakia with metaphyseal dysplasia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Microspherophakia with metaphyseal dysplasia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Ulnar dimelia	Occurrence	True	Congenital	Inferred relationship	Some	1
Right descending aorta	Occurrence	True	Congenital	Inferred relationship	Some	1
Atrioventricular septal defect with ventricular component under superior bridging leaflet without chordal attachment to ventricular septal crest (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Endocardial fibroelastosis of left atrium (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Segmental neurofibromatosis	Occurrence	True	Congenital	Inferred relationship	Some	1
albinoidism	Occurrence	False	Congenital	Inferred relationship	Some	1
Incomplete bilateral cleft palate	Occurrence	True	Congenital	Inferred relationship	Some	1
syndrom med kraniosynostos med ansiktsmissbildning och brakydaktyli	Occurrence	False	Congenital	Inferred relationship	Some	3
syndrom med kraniosynostos med ansiktsmissbildning och brakydaktyli	Occurrence	False	Congenital	Inferred relationship	Some	1
syndrom med kraniosynostos med ansiktsmissbildning och brakydaktyli	Occurrence	False	Congenital	Inferred relationship	Some	2
Townes syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Epidermolysis bullosa simplex with hypodontia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Talipomanus	Occurrence	True	Congenital	Inferred relationship	Some	1
Mixed sclerosing bone dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleidocranial dysostosis	Occurrence	True	Congenital	Inferred relationship	Some	3
Cleidocranial dysostosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Cleidocranial dysostosis	Occurrence	True	Congenital	Inferred relationship	Some	4
Cleidocranial dysostosis	Occurrence	True	Congenital	Inferred relationship	Some	2
Retrocaval ureter	Occurrence	True	Congenital	Inferred relationship	Some	1
Chondrodysplasia punctata	Occurrence	True	Congenital	Inferred relationship	Some	1
Cataract glaucoma syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
X-linked distal arthrogryposis multiplex congenita (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Nemaline myopathy	Occurrence	True	Congenital	Inferred relationship	Some	1
Hydatid cyst of Morgagni - male	Occurrence	True	Congenital	Inferred relationship	Some	1
Birthmark	Occurrence	True	Congenital	Inferred relationship	Some	1
Incomplete ossification of maxilla	Occurrence	True	Congenital	Inferred relationship	Some	1
syndrom med sparsam hårväxt, kortvuxenhet och missbildning i huden	Occurrence	False	Congenital	Inferred relationship	Some	1
syndrom med sparsam hårväxt, kortvuxenhet och missbildning i huden	Occurrence	False	Congenital	Inferred relationship	Some	2
Siegler Brewer Carey syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Spondylodysplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Spina bifida with stenosis of aqueduct of Sylvius	Occurrence	True	Congenital	Inferred relationship	Some	3
Ectodermal dysplasia with hair-tooth defects	Occurrence	True	Congenital	Inferred relationship	Some	1
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Sialic acid storage disease, severe infantile type	Occurrence	True	Congenital	Inferred relationship	Some	1
Epidermolysis bullosa	Occurrence	True	Congenital	Inferred relationship	Some	1
Stimmler syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Stimmler syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Osteopathia striata	Occurrence	True	Congenital	Inferred relationship	Some	1
False tendon - heart	Occurrence	True	Congenital	Inferred relationship	Some	1
Double cardiac valve orifice	Occurrence	True	Congenital	Inferred relationship	Some	1
Netherton's syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital arteriovenous fistula thrombosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Craniopagus	Occurrence	False	Congenital	Inferred relationship	Some	1
Retrosternal thyroid gland	Occurrence	True	Congenital	Inferred relationship	Some	1
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Synophrys	Occurrence	True	Congenital	Inferred relationship	Some	1
Crouzon syndrome with acanthosis nigricans (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Crouzon syndrome with acanthosis nigricans (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Cataract, congenital heart disease, neural tube defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Cataract, congenital heart disease, neural tube defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cataract, congenital heart disease, neural tube defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	4
Cataract, congenital heart disease, neural tube defect syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Multiple epiphyseal dysplasia Beighton type (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Odontomicronychial ectodermal dysplasia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cherubism with gingival fibromatosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Dolichocolon	Occurrence	True	Congenital	Inferred relationship	Some	1

Start Previous Page 269 of 322 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)