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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
Congenital vascular anomaly of lower eyelid Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Chronic granulomatous disease Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Temporal encephalocele Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lumbar meningomyelocele Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Lumbar meningomyelocele Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Lumbar meningomyelocele Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Parietal encephalocele Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital cerebral meningocele Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital cerebral meningocele Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Spina bifida of lumbar region Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital protrusion of tongue Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital sacral meningocele with conotruncal heart defect syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Low lumbar myelomeningocele Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cervical myelocele Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cervical myelocele Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital cerebral hernia Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hydromeningocele - cranial Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Thoracic myelocele Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Dens evaginatus Occurrence False Congenital Inferred relationship Existential restriction modifier 1
High lumbar myelomeningocele Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lumbar myelocele Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lumbar myelocele Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Lumbar spina bifida without hydrocephalus - closed Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Thoracic meningomyelocele Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Thoracic meningomyelocele Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Thoracic meningomyelocele Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Congenital abnormal long growth of bile duct Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cervical meningomyelocele Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Cervical meningomyelocele Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cervical meningomyelocele Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Bilateral medullary sponge kidney Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital onychauxis Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Navajo neurohepatopathy Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Navajo neurohepatopathy Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Familial congenital mirror movements Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Antecubital pterygium syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pulmonary valve agenesis, intact ventricular septum, persistent ductus arteriosus syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pulmonary valve agenesis, intact ventricular septum, persistent ductus arteriosus syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Craniorhiny Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Craniorhiny Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Craniorhiny Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Developmental dislocation of ankle and/or foot Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Developmental dislocation of ankle and/or foot Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Developmental dislocation of joint of shoulder region Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Developmental dislocation of joint of shoulder region Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital single renal cyst Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Ectopic artery Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Autosomal recessive cutis laxa type 2A Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Autosomal recessive cutis laxa type 2A Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Posterior fossa arachnoid cyst Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Atrioventricular septal defect with atrioventricular valve regurgitation through right anterosuperior inferior mural commissure Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with atrioventricular valve regurgitation through right anterosuperior superior bridging leaflet commissure Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with atrioventricular valve regurgitation through right inferior bridging leaflet inferior mural commissure Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital cystic disease of liver Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with atrioventricular valve regurgitation through left septal commissure Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with atrioventricular valve regurgitation through left superior bridging leaflet lateral mural commissure Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with atrioventricular valve regurgitation through right septal commissure Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital vesicoureterorenal reflux, bilateral Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Atrioventricular septal defect with atrioventricular valve regurgitation through left inferior bridging leaflet lateral mural commissure Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Atrioventricular septal defect with atrioventricular valve regurgitation Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Multiple congenital anomalies, hypotonia, seizures syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Multiple congenital anomalies, hypotonia, seizures syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Multiple congenital anomalies, hypotonia, seizures syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Muscle eye brain disease with bilateral multicystic leukodystrophy Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Muscle eye brain disease with bilateral multicystic leukodystrophy Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Cobblestone lissencephaly without muscular or ocular involvement Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 24 Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 8 Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Hypertrophic Meckel's diverticulum Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pachyonychia congenita syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Obesity due to leptin receptor gene deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Obesity due to leptin receptor gene deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Branchial cleft sinus and fistula Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Fistula of branchial cleft Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Aneurysm osteoarthritis syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Aneurysm osteoarthritis syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Fordyce's disease Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Fordyce spots of lips Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Bilateral multicystic renal dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Lethal arthrogryposis co-occurrent with anterior horn cell disease Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Distal arthrogryposis type 4 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Lethal congenital contracture syndrome type 2 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital anomaly of right optic disc Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital anomaly of bilateral optic discs Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital anomaly of bilateral optic discs Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital anomaly of left optic disc Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Fistula colli congenita Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Arthrogryposis and ectodermal dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Arthrogryposis and ectodermal dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Arthrogryposis and ectodermal dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Arthrogryposis and ectodermal dysplasia syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Congenital systemic arteriovenous fistula Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Microphthalmos of right eye Occurrence True Congenital Inferred relationship Existential restriction modifier 1

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