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255399007: Congenital (qualifier value)

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

Descriptions:

Id Description Lang Type Status Case? Module
273731000077117 congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
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
554801000077113 congénital (valeur de l'attribut) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
646433016 Congenital (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
congénital est un(e) (attribut) périodes de vie true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Unilateral cartilaginous centrum of sacral vertebra survenue (attribut) False congénital Inferred relationship Some
Unilateral cartilaginous centrum of thoracic vertebra survenue (attribut) False congénital Inferred relationship Some
Distichiasis survenue (attribut) False congénital Inferred relationship Some
Hypertrophy of right kidney co-occurrent and due to congenital hypoplasia of left kidney survenue (attribut) True congénital Inferred relationship Some 1
Juvenile GM2 gangliosidosis (disorder) survenue (attribut) False congénital Inferred relationship Some 3
Immunodeficiency due to ficolin 3 deficiency (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Isochromosomy Yp survenue (attribut) True congénital Inferred relationship Some 1
Isolated cerebellar vermis hypoplasia survenue (attribut) True congénital Inferred relationship Some 1
Cortical dysplasia survenue (attribut) True congénital Inferred relationship Some 1
Cortical dysplasia with hemimegalencephaly survenue (attribut) True congénital Inferred relationship Some 1
Paternal uniparental disomy of chromosome 21 (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Metabolic myopathy due to lactate transporter defect survenue (attribut) True congénital Inferred relationship Some 1
Monosomy 13q34 syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Monosomy 13q34 syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
dysplasie épiphysaire multiple due à une anomalie du collagène 9 survenue (attribut) True congénital Inferred relationship Some 1
Paternal uniparental disomy of chromosome 1 (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Paternal uniparental disomy of chromosome 7 survenue (attribut) True congénital Inferred relationship Some 1
Localized cortical dysplasia survenue (attribut) True congénital Inferred relationship Some 1
Isolated focal cortical dysplasia (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Cervical rib syndrome survenue (attribut) False congénital Inferred relationship Some
Anomaly of sex chromosome survenue (attribut) False congénital Inferred relationship Some
Congenital anomaly of joint survenue (attribut) False congénital Inferred relationship Some
Congenital absence of cranial vault survenue (attribut) False congénital Inferred relationship Some
Congenital claw toe survenue (attribut) False congénital Inferred relationship Some
Congenital perforation of nasal septum survenue (attribut) False congénital Inferred relationship Some
Congenital tracheomalacia survenue (attribut) False congénital Inferred relationship Some
Nijmegen breakage syndrome-like disorder (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Nijmegen breakage syndrome-like disorder (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Congenital bronchomalacia survenue (attribut) False congénital Inferred relationship Some
Multiple epiphyseal dysplasia with miniepiphyses survenue (attribut) True congénital Inferred relationship Some 1
Neuhauser anomaly survenue (attribut) True congénital Inferred relationship Some 1
Abnormal plantar creases survenue (attribut) False congénital Inferred relationship Some
Tetrasomy 5p syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Congenital anomaly of digestive tract survenue (attribut) False congénital Inferred relationship Some
Subaortic course of innominate vein survenue (attribut) True congénital Inferred relationship Some 1
Congenital arteriovenous malformation of gastrointestinal tract (disorder) survenue (attribut) False congénital Inferred relationship Some
Multiple gastrointestinal atresias survenue (attribut) False congénital Inferred relationship Some
Congenital anomaly of jaw survenue (attribut) False congénital Inferred relationship Some
Congenital vesico-ureteric reflux survenue (attribut) False congénital Inferred relationship Some
Congenital degeneration of nervous system survenue (attribut) False congénital Inferred relationship Some
Congenital sacral meningocele survenue (attribut) False congénital Inferred relationship Some
Congenital sclerocornea survenue (attribut) False congénital Inferred relationship Some
Anterior lenticonus survenue (attribut) False congénital Inferred relationship Some
Anterior lentiglobus survenue (attribut) False congénital Inferred relationship Some
Posterior lenticonus survenue (attribut) False congénital Inferred relationship Some
Posterior lentiglobus survenue (attribut) False congénital Inferred relationship Some
Congenital pigmentation of lens survenue (attribut) False congénital Inferred relationship Some
Congenital anterior capsular pigmentation survenue (attribut) False congénital Inferred relationship Some
Congenital blindness survenue (attribut) False congénital Inferred relationship Some
Congenital macular corneal dystrophy survenue (attribut) False congénital Inferred relationship Some
Congenital conjunctival cyst survenue (attribut) False congénital Inferred relationship Some
Congenital anomaly of choroid survenue (attribut) False congénital Inferred relationship Some
Congenital hypoplasia of choroid survenue (attribut) False congénital Inferred relationship Some
Congenital hypopigmentation of choroid survenue (attribut) False congénital Inferred relationship Some
Congenital retinoschisis survenue (attribut) False congénital Inferred relationship Some
Retinal dysplasia survenue (attribut) False congénital Inferred relationship Some
Multifocal retinal dysplasia survenue (attribut) False congénital Inferred relationship Some
Geographic retinal dysplasia survenue (attribut) False congénital Inferred relationship Some
Diffuse retinal dysplasia survenue (attribut) False congénital Inferred relationship Some
Congenital myelin deficiency of the optic disc survenue (attribut) False congénital Inferred relationship Some
Hypoplasia of the optic nerve survenue (attribut) False congénital Inferred relationship Some
Isolated unilateral hemispheric cerebellar hypoplasia (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 4
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Persistent pupillary membranes survenue (attribut) False congénital Inferred relationship Some
Carney complex, trismus, pseudocamptodactyly syndrome survenue (attribut) True congénital Inferred relationship Some 3
Carney complex, trismus, pseudocamptodactyly syndrome survenue (attribut) True congénital Inferred relationship Some 2
Carney complex, trismus, pseudocamptodactyly syndrome survenue (attribut) True congénital Inferred relationship Some 1
Trichoodontoonychial dysplasia survenue (attribut) True congénital Inferred relationship Some 2
Trichoodontoonychial dysplasia survenue (attribut) True congénital Inferred relationship Some 1
Trichoodontoonychial dysplasia survenue (attribut) True congénital Inferred relationship Some 3
Trichoodontoonychial dysplasia survenue (attribut) True congénital Inferred relationship Some 4
Diencephalic mesencephalic junction dysplasia (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Diencephalic mesencephalic junction dysplasia (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Retinal arteriovenous malformation survenue (attribut) False congénital Inferred relationship Some
Congenital anomaly of optic nerve survenue (attribut) False congénital Inferred relationship Some
Cono-spondylar dysplasia (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Cono-spondylar dysplasia (disorder) survenue (attribut) True congénital Inferred relationship Some 1
paraplégie spastique autosomique récessive type 67 survenue (attribut) False congénital Inferred relationship Some 2
paraplégie spastique autosomique récessive type 67 survenue (attribut) False congénital Inferred relationship Some 1
Trichodysplasia xeroderma syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Macropalpebral fissure survenue (attribut) False congénital Inferred relationship Some
Trichodysplasia xeroderma syndrome (disorder) survenue (attribut) False congénital Inferred relationship Some 1
Ectopic cilia of eyelid survenue (attribut) False congénital Inferred relationship Some
Combined immunodeficiency due to OX40 deficiency survenue (attribut) True congénital Inferred relationship Some 1
2q23.1 microduplication syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Short stature due to growth hormone secretagogue receptor deficiency survenue (attribut) False congénital Inferred relationship Some 1
Congenitally small punctum lacrimale survenue (attribut) False congénital Inferred relationship Some
X-linked non progressive cerebellar ataxia (disorder) survenue (attribut) False congénital Inferred relationship Some 1
Familial lambdoid synostosis survenue (attribut) False congénital Inferred relationship Some 2
Familial lambdoid synostosis survenue (attribut) False congénital Inferred relationship Some 1
Severe lateral tibial bowing with short stature survenue (attribut) True congénital Inferred relationship Some 1
Severe lateral tibial bowing with short stature survenue (attribut) True congénital Inferred relationship Some 2
Epiphyseal dysplasia survenue (attribut) True congénital Inferred relationship Some 1
Congenital displacement of punctum lacrimale survenue (attribut) False congénital Inferred relationship Some
dysplasie spondylo-épimétaphysaire avec luxations multiples survenue (attribut) True congénital Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2

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