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
Persistence of primitive artery	Occurrence	True	Congenital	Inferred relationship	Some	1
Venous valvular anomaly	Occurrence	True	Congenital	Inferred relationship	Some	1
Deep vein aplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Deep vein hypoplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Capillary-venous malformation	Occurrence	True	Congenital	Inferred relationship	Some	2
Venous-lymphatic malformation	Occurrence	True	Congenital	Inferred relationship	Some	2
Capillary-venous-lymphatic malformation	Occurrence	True	Congenital	Inferred relationship	Some	3
Congenital arteriovenous malformation	Occurrence	True	Congenital	Inferred relationship	Some	1
Cerebral arteriovenous malformation	Occurrence	True	Congenital	Inferred relationship	Some	1
Parkes Weber syndrome	Occurrence	False	Congenital	Inferred relationship	Some	5
Congenital arteriovenous fistula	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital arteriovenous fistula of brain	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital arteriovenous fistula occlusion	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital arteriovenous fistula stenosis	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital arteriovenous fistula thrombosis	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital arteriovenous fistula infection	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital arteriovenous fistula aneurysm	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital arteriovenous fistula haemorrhage	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital arteriovenous fistula rupture	Occurrence	True	Congenital	Inferred relationship	Some	2
Specific mixed vascular syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Amelogenesis imperfecta - hypoplastic autosomal dominant - local	Occurrence	True	Congenital	Inferred relationship	Some	1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth	Occurrence	True	Congenital	Inferred relationship	Some	1
Amelogenesis imperfecta - hypoplastic autosomal dominant - rough	Occurrence	True	Congenital	Inferred relationship	Some	1
Amelogenesis imperfecta - recessive - rough	Occurrence	True	Congenital	Inferred relationship	Some	1
Amelogenesis imperfecta - hypomaturation - recessive pigmented	Occurrence	True	Congenital	Inferred relationship	Some	1
Amelogenesis imperfecta - hypomaturation - snow capped teeth	Occurrence	True	Congenital	Inferred relationship	Some	1
Dentinogenesis imperfecta - Shield's type I	Occurrence	True	Congenital	Inferred relationship	Some	1
Dentinogenesis imperfecta - Shield's type II	Occurrence	True	Congenital	Inferred relationship	Some	1
Dentinogenesis imperfecta - Shield's type III	Occurrence	True	Congenital	Inferred relationship	Some	1
Midline sinus of the upper lip	Occurrence	True	Congenital	Inferred relationship	Some	1
Malrotation of the intestine type IA	Occurrence	True	Congenital	Inferred relationship	Some	1
Malrotation of the intestine type IIA (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Malrotation of the intestine type IIB	Occurrence	True	Congenital	Inferred relationship	Some	1
Malrotation of the intestine type IIC	Occurrence	True	Congenital	Inferred relationship	Some	1
Malrotation of the intestine type IIIA	Occurrence	True	Congenital	Inferred relationship	Some	1
Malrotation of the intestine type IIIB	Occurrence	True	Congenital	Inferred relationship	Some	1
Ichthyosis congenita with biliary atresia	Occurrence	True	Congenital	Inferred relationship	Some	2
Polycystic disease of pancreas	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital malformation of pancreas	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital umbilical defect	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital renal artery aneurysm	Occurrence	True	Congenital	Inferred relationship	Some	1
Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Primary vesicoureteric reflux	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital abnormality of scrotum	Occurrence	True	Congenital	Inferred relationship	Some	1
Bifid scrotum	Occurrence	True	Congenital	Inferred relationship	Some	1
uterus bicornis som komplicerar postpartumvård, barnet framfött under tidigare vårdperiod	Occurrence	False	Congenital	Inferred relationship	Some	1
uterus bicornis som komplicerar mödravården, barnet ännu inte framfött	Occurrence	False	Congenital	Inferred relationship	Some	1
uterus bicornis, barnet framfött med postpartumkomplikation	Occurrence	False	Congenital	Inferred relationship	Some	1
uterus bicornis, barnet framfött	Occurrence	False	Congenital	Inferred relationship	Some	1
Bicornuate uterus affecting obstetric care	Occurrence	True	Congenital	Inferred relationship	Some	1
Bicornuate uterus in pregnancy, childbirth and the puerperium	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital heart disease in pregnancy	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital anomaly of bone and joint	Occurrence	True	Congenital	Inferred relationship	Some	2
Congenital thyroid hypoplasia	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital adrenal hypoplasia, X-linked	Occurrence	True	Congenital	Inferred relationship	Some	1
Waardenburg syndrome type 3 (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Genodermatosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Multiple benign annular creases of extremities	Occurrence	True	Congenital	Inferred relationship	Some	1
Reticulate pigmented anomaly of flexures	Occurrence	True	Congenital	Inferred relationship	Some	1
Hereditary clubbing	Occurrence	False	Congenital	Inferred relationship	Some	1
Cutaneous syndrome with ichthyosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Keratitis ichthyosis and deafness syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Atypical ichthyosis vulgaris with hypogonadism	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital erector pili hamartoma	Occurrence	True	Congenital	Inferred relationship	Some	1
Diffuse smooth muscle hamartoma	Occurrence	True	Congenital	Inferred relationship	Some	1
X-linked muscular dystrophy with limb girdle distribution	Occurrence	False	Congenital	Inferred relationship	Some	2
X-linked muscular dystrophy with abnormal dystrophin	Occurrence	False	Congenital	Inferred relationship	Some	2
Intermediate X-linked muscular dystrophy	Occurrence	False	Congenital	Inferred relationship	Some	2
Manifesting female carrier of X-linked muscular dystrophy	Occurrence	False	Congenital	Inferred relationship	Some	2
X-linked limb girdle muscular dystrophy with normal dystrophin	Occurrence	False	Congenital	Inferred relationship	Some	2
Jis muskeldystrofi	Occurrence	False	Congenital	Inferred relationship	Some	2
Hereditary myopathy limited to females	Occurrence	False	Congenital	Inferred relationship	Some	2
Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein	Occurrence	True	Congenital	Inferred relationship	Some	2
autosomalt recessiv muskeldystrofi med gen belägen på 15q	Occurrence	False	Congenital	Inferred relationship	Some	2
Reunion-Indiana Amish type muscular dystrophy	Occurrence	False	Congenital	Inferred relationship	Some	2
Hutterite type of muscular dystrophy	Occurrence	False	Congenital	Inferred relationship	Some	2
X-linked muscular dystrophy not predominantly limb girdle	Occurrence	False	Congenital	Inferred relationship	Some	2
benign skapuloperoneal muskeldystrofi med kardiomyopati	Occurrence	False	Congenital	Inferred relationship	Some	2
Autosomal recessive muscular dystrophy not predominantly limb girdle	Occurrence	False	Congenital	Inferred relationship	Some	2
Scapulohumeral muscular dystrophy	Occurrence	False	Congenital	Inferred relationship	Some	2
Autosomal dominant muscular dystrophy not predominantly limb girdle	Occurrence	False	Congenital	Inferred relationship	Some	2
Benign scapuloperoneal muscular dystrophy	Occurrence	False	Congenital	Inferred relationship	Some	2
Benign congenital muscular dystrophy with finger flexion contractures	Occurrence	False	Congenital	Inferred relationship	Some	2
Autosomal recessive centronuclear myopathy	Occurrence	True	Congenital	Inferred relationship	Some	1
Myopathy with abnormality of histochemical fibre type	Occurrence	True	Congenital	Inferred relationship	Some	1
Myopathy with type I hypotrophy	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital myopathy with fibre type disproportion	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital myopathy with uniform fiber type	Occurrence	True	Congenital	Inferred relationship	Some	1
Myopathy with cytoplasmic inclusions	Occurrence	True	Congenital	Inferred relationship	Some	1
Myopathy with tubular aggregates	Occurrence	True	Congenital	Inferred relationship	Some	1
Morning glory disc	Occurrence	True	Congenital	Inferred relationship	Some	1
vaskulär anomali i synnervspapill	Occurrence	False	Congenital	Inferred relationship	Some	1
Flat birthmark	Occurrence	True	Congenital	Inferred relationship	Some	2
aberrant artär	Occurrence	False	Congenital	Inferred relationship	Some	1
Bicuspid doming of aortic cusp	Occurrence	True	Congenital	Inferred relationship	Some	1
Aortic root congenital abnormality	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital malformation of angle of anterior chamber of eye	Occurrence	True	Congenital	Inferred relationship	Some	1
Barkan membrane (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Abnormality of neurogenesis	Occurrence	True	Congenital	Inferred relationship	Some	1
Lobar holoprosencephaly	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)