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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
Gnathodiaphyseal dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cervical spina bifida with hydrocephalus - open Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Cervical spina bifida with hydrocephalus - open Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Parastremmatic dwarfism Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Complete transposition of great vessels Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Complete transposition of great vessels Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Popliteal pterygium syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Shprintzen Goldberg craniosynostosis syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Shprintzen Goldberg craniosynostosis syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Taurodontia with absent teeth and sparse hair syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Taurodontia with absent teeth and sparse hair syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Taurodontia with absent teeth and sparse hair syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 8 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ectodermal dysplasia with acanthosis nigricans syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Brachydactylous dwarfism Mseleni type Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Interatrial communication through coronary sinus orifice Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Keratin 14 related epidermolysis bullosa simplex Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Incomplete ossification of fibula Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Imperforate jejunum Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital atrial septal defect Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lymphedema, atrial septal defect, facial changes syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Lymphedema, atrial septal defect, facial changes syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Joubert syndrome with ocular defect Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Supernumerary roots Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Congenital bronchoesophageal fistula without atresia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cleft lip and cleft palate with ectodermal dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Melnick-Needles syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hemicentric sacral centrum Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Congenital cataract with ataxia and deafness syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Thoracolumbar spina bifida with hydrocephalus - closed Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Nevus comedonicus Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Multiple synostosis syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Longitudinal absence of radius AND ulna Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Longitudinal absence of radius AND ulna Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Port-wine stain associated with spinal dysraphism Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Port-wine stain associated with spinal dysraphism Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Flynn-Aird syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Curry-Hall syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Marshall syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Acrocephalopolysyndactyly type IV Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Acrocephalopolysyndactyly type IV Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Vascular ring with left aortic arch to right descending aorta and right patent arterial duct Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Immuno-osseous dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Radial hypoplasia and triphalangeal thumb with hypospadias and maxillary diastema syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Hypohidrosis with neurolabyrinthitis Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Manus valga Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Spina bifida aperta of thoracic spine Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Spina bifida aperta of thoracic spine Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hypohidrotic X-linked ectodermal dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Smith Fineman Myers syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Carbohydrate sulfotransferase 3 related skeletal dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Dappled diaphyseal dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cutis gyrata syndrome of Beare and Stevenson Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Juvenile fucosidosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital stricture of osseous meatus Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Familial multiple café-au-lait macules without neurofibromatosis Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Syndromic recessive X-linked ichthyosis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Osseous syndactyly of toes second to fourth web Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Mobile kidney Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hydrocephalus, cardiac malformation, dense bone syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Hydrocephalus, cardiac malformation, dense bone syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Vascular loops of inner ear Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Camptodactyly taurinuria syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Craniopagus parasiticus Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Brachyolmia - Hobaek type Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Omphalocele with obstruction Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Dicephalus tripus tribrachius Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deafness with skeletal dysplasia and lip granuloma syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deafness with skeletal dysplasia and lip granuloma syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Pseudohypoparathyroidism type I A Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Spondyloepimetaphyseal dysplasia with joint laxity Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Greig cephalopolysyndactyly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Bosley Salih Alorainy syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Neurofaciodigitorenal syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Neurofaciodigitorenal syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Pili annulati Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Mesomelic dysplasia Kantaputra type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital microgastria with limb reduction defect syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cleidorhizomelic syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Seckel syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Seckel syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Craniopagus occipitalis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Arthrogryposis hyperkeratosis syndrome lethal form Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Arthrogryposis hyperkeratosis syndrome lethal form Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital vascular malformation due to inherited syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hypertaurodontism Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Left ventricular outflow tract obstruction due to diaphragm Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Vertical retraction syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Microgyria Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Severe generalized recessive dystrophic epidermolysis bullosa Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital micrognathism Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hand-foot-genital syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1

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