FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.2  |  FHIR Version n/a  User: [n/a]

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
46,XX disorder of sex development with anorectal anomalies syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Atrioventricular septal defect with ventricular component under superior bridging leaflet with chords at crest ventricular septum (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 2 (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Double eyebrow survenue (attribut) True congénital Inferred relationship Some 1
Incomplete ossification of centrum of cervical vertebra survenue (attribut) True congénital Inferred relationship Some 1
Congenital rectocloacal fistula survenue (attribut) True congénital Inferred relationship Some 1
Severe autosomal recessive muscular dystrophy of childhood - North African type survenue (attribut) False congénital Inferred relationship Some 2
Congenital abnormality of left atrioventricular valve chordae tendinae in double inlet ventricle (disorder) survenue (attribut) True congénital Inferred relationship Some 1
syndrome de déficience intellectuelle liée à l'X-dysmorphie-atrophie cérébrale survenue (attribut) True congénital Inferred relationship Some 1
Congenital anomalies of eyelid, lacrimal system and orbit survenue (attribut) True congénital Inferred relationship Some 1
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 4
Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Coxoauricular syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Coxoauricular syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Congenital calculus of kidney (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Trigonocephaly, short stature, developmental delay syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Thoracolumbar spina bifida without hydrocephalus - closed survenue (attribut) True congénital Inferred relationship Some 2
Congenital hypoplasia of nasal septum survenue (attribut) False congénital Inferred relationship Some 1
Intracardiac location of anomalous pulmonary venous connection to coronary sinus (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Venous-lymphatic malformation survenue (attribut) True congénital Inferred relationship Some 1
Myelomeningocele co-occurrent with hydrocephalus (disorder) survenue (attribut) True congénital Inferred relationship Some 4
Myelomeningocele co-occurrent with hydrocephalus (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Myelomeningocele co-occurrent with hydrocephalus (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Myelomeningocele co-occurrent with hydrocephalus (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Sclerosteosis survenue (attribut) True congénital Inferred relationship Some 1
Arachnodactyly and intellectual disability with facial dysmorphism syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Pulmonary venous confluence in direct proximity to left atrium (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Pyknodysostosis survenue (attribut) True congénital Inferred relationship Some 1
Early onset myopathy with fatal cardiomyopathy (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Incomplete ossification of talus survenue (attribut) True congénital Inferred relationship Some 1
Pericarditis secondary to Mulibrey nanism survenue (attribut) True congénital Inferred relationship Some 2
Thrombocythemia with distal limb defect (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Cervical rib survenue (attribut) True congénital Inferred relationship Some 1
Ectodermal dysplasia with tooth-sweating defect survenue (attribut) True congénital Inferred relationship Some 1
Ehlers-Danlos syndrome vascular-like type (disorder) survenue (attribut) False congénital Inferred relationship Some 2
Ehlers-Danlos syndrome vascular-like type (disorder) survenue (attribut) False congénital Inferred relationship Some 1
Radial polydactyly Wassel 3 survenue (attribut) False congénital Inferred relationship Some 1
encéphalopathie épileptique avec démyélinisation cérébrale généralisée survenue (attribut) True congénital Inferred relationship Some 1
Uterus acollis survenue (attribut) True congénital Inferred relationship Some 1
Intellectual disability with cataract and kyphosis syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Intellectual disability with cataract and kyphosis syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
syndrome de maladie de Hirschsprung-brachydactylie type D survenue (attribut) True congénital Inferred relationship Some 3
syndrome de maladie de Hirschsprung-brachydactylie type D survenue (attribut) True congénital Inferred relationship Some 1
syndrome de maladie de Hirschsprung-brachydactylie type D survenue (attribut) True congénital Inferred relationship Some 2
Axillary freckling due to neurofibromatosis (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Axillary freckling due to neurofibromatosis (disorder) survenue (attribut) False congénital Inferred relationship Some 1
Mondini defect survenue (attribut) True congénital Inferred relationship Some 1
camptodactylie de Tel Hashomer survenue (attribut) True congénital Inferred relationship Some 2
camptodactylie de Tel Hashomer survenue (attribut) True congénital Inferred relationship Some 3
camptodactylie de Tel Hashomer survenue (attribut) True congénital Inferred relationship Some 1
Amelogenesis imperfecta, hypoplastic type with microdontia survenue (attribut) True congénital Inferred relationship Some 1
Trifid pelvis of kidney (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 5
Oesophageal atresia, stenosis and fistula survenue (attribut) True congénital Inferred relationship Some 1
Greenberg dysplasia (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Thanatophoric dysplasia, type 1 (disorder) survenue (attribut) True congénital Inferred relationship Some 1
chondrodysplasie métaphysaire type Schmid (trouble) survenue (attribut) True congénital Inferred relationship Some 1
Deformity of digit of hand due to amniotic band (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Oesophageal atresia with tracheo-oesophageal fistula survenue (attribut) True congénital Inferred relationship Some 2
Steroid dehydrogenase deficiency and dental anomaly syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Craniotabes survenue (attribut) True congénital Inferred relationship Some 1
syndrome de dysplasie osseuse terminale-défauts de pigmentation survenue (attribut) True congénital Inferred relationship Some 1
Congenital absence of forearm and hand survenue (attribut) False congénital Inferred relationship Some 3
Congenital absence of forearm and hand survenue (attribut) True congénital Inferred relationship Some 2
Congenital absence of forearm and hand survenue (attribut) True congénital Inferred relationship Some 1
Tetraamelia with multiple malformation syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Bipartite ossification of centrum of cervical vertebra survenue (attribut) True congénital Inferred relationship Some 1
Short rib polydactyly syndrome type I (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Short rib polydactyly syndrome type I (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Short rib polydactyly syndrome type I (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Short rib polydactyly syndrome type I (disorder) survenue (attribut) False congénital Inferred relationship Some 4
syndrome de Ruvalcaba (trouble) survenue (attribut) True congénital Inferred relationship Some 1
Proximal femoral focal deficiency survenue (attribut) True congénital Inferred relationship Some 1
Caudal appendage deafness syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3
Caudal appendage deafness syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Caudal appendage deafness syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Common arterial trunk with aortic dominance (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Brachydactyly and arterial hypertension syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Triplication of appendix survenue (attribut) True congénital Inferred relationship Some 1
Dyschondrosteosis and nephritis syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Dyschondrosteosis and nephritis syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Manus extensa survenue (attribut) False congénital Inferred relationship Some 2
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 2
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 1
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) survenue (attribut) True congénital Inferred relationship Some 3

Start Previous Page 27 of 326 Next End

This concept is not in any reference sets

Back to Start