FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.9.0  |  FHIR Version n/a  User: [n/a]

255399007: Congenital (qualifier value)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
380598010 Congenital en Synonym Active Case insensitive SNOMED CT core
380599019 Congenita en Synonym Active Case insensitive SNOMED CT core
646433016 Congenital (qualifier value) en Fully specified name Active Case insensitive SNOMED CT core

0 descendants.

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
McCune Albright syndrome Occurrence False Congenital Inferred relationship Some 6
McCune Albright syndrome Occurrence False Congenital Inferred relationship Some 7
CAMOS syndrome Occurrence True Congenital Inferred relationship Some 3
CAMOS syndrome Occurrence False Congenital Inferred relationship Some 4
CAMOS syndrome Occurrence False Congenital Inferred relationship Some 5
Congenital myotonia Occurrence True Congenital Inferred relationship Some 1
Congenital sacral meningocele Occurrence True Congenital Inferred relationship Some 1
Neurofaciodigitorenal syndrome Occurrence True Congenital Inferred relationship Some 3
Neurofaciodigitorenal syndrome Occurrence False Congenital Inferred relationship Some 4
Neurofaciodigitorenal syndrome Occurrence False Congenital Inferred relationship Some 5
Hereditary hypercarotenaemia and vitamin A deficiency Occurrence True Congenital Inferred relationship Some 1
Kousseff syndrome Occurrence False Congenital Inferred relationship Some 4
Kousseff syndrome Occurrence False Congenital Inferred relationship Some 5
Kousseff syndrome Occurrence False Congenital Inferred relationship Some 6
X-linked diffuse leiomyomatosis with Alport syndrome Occurrence True Congenital Inferred relationship Some 3
X-linked diffuse leiomyomatosis with Alport syndrome Occurrence True Congenital Inferred relationship Some 4
X-linked diffuse leiomyomatosis with Alport syndrome Occurrence True Congenital Inferred relationship Some 5
Distal myopathy Welander type Occurrence False Congenital Inferred relationship Some 2
Distal myopathy Welander type Occurrence False Congenital Inferred relationship Some 3
Patent ductus arteriosus with left-to-right shunt Occurrence False Congenital Inferred relationship Some
Patent ductus arteriosus with right-to-left shunt Occurrence False Congenital Inferred relationship Some
Cutis marmorata Occurrence False Congenital Inferred relationship Some 2
Reticulate vascular naevus Occurrence True Congenital Inferred relationship Some 1
Naevus sanguineous Occurrence True Congenital Inferred relationship Some 1
Mixed haemangioma Occurrence True Congenital Inferred relationship Some 1
Congenital livedo reticularis Occurrence True Congenital Inferred relationship Some 1
Congenital anomaly of descending thoracic aorta Occurrence True Congenital Inferred relationship Some 1
Congenital anomaly of abdominal aorta Occurrence True Congenital Inferred relationship Some 1
Compression of trachea and oesophagus co-occurrent and due to congenital anomaly of aortic arch Occurrence False Congenital Inferred relationship Some 4
Compression of trachea and oesophagus co-occurrent and due to congenital anomaly of aortic arch Occurrence False Congenital Inferred relationship Some 5
Compression of trachea and oesophagus co-occurrent and due to congenital anomaly of aortic arch Occurrence False Congenital Inferred relationship Some 6
Congenital precerebral nonruptured aneurysm Occurrence False Congenital Inferred relationship Some 1
Myeloid leukaemia co-occurrent with Down syndrome Occurrence False Congenital Inferred relationship Some 5
Suprabasal epidermolysis bullosa simplex Occurrence False Congenital Inferred relationship Some 4
Suprabasal epidermolysis bullosa simplex Occurrence False Congenital Inferred relationship Some 5
Congenital venous malformation of skin Occurrence False Congenital Inferred relationship Some 2
Cystic hygroma in fetus Occurrence False Congenital Inferred relationship Some 5
Ataxia co-occurrent and due to phytanic acid storage disease Occurrence True Congenital Inferred relationship Some 5
Keratinopathic ichthyosis Occurrence True Congenital Inferred relationship Some 1
Hereditary skin peeling syndrome Occurrence False Congenital Inferred relationship Some 5
Cystic hygroma in fetus Occurrence False Congenital Inferred relationship Some 6
Isolated optic nerve hypoplasia Occurrence True Congenital Inferred relationship Some 1
Short rib polydactyly syndrome Saldino Noonan type Occurrence False Congenital Inferred relationship Some 5
Short rib polydactyly syndrome Saldino Noonan type Occurrence False Congenital Inferred relationship Some 6
Short rib polydactyly syndrome Saldino Noonan type Occurrence False Congenital Inferred relationship Some 7
Short rib polydactyly syndrome Saldino Noonan type Occurrence False Congenital Inferred relationship Some 8
X-linked hereditary spastic paraplegia Occurrence False Congenital Inferred relationship Some 6
Right metatarsus adductus Occurrence True Congenital Inferred relationship Some 1
Left metatarsus adductus Occurrence True Congenital Inferred relationship Some 1
Multiple malformation syndrome with senile-like appearance Occurrence False Congenital Inferred relationship Some
Talocalcaneal coalition Occurrence False Congenital Inferred relationship Some
Congenital anomaly of perineum Occurrence False Congenital Inferred relationship Some
Congenital anomaly of intestinal tract Occurrence False Congenital Inferred relationship Some
X-linked hereditary spastic paraplegia Occurrence False Congenital Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 32 Occurrence False Congenital Inferred relationship Some
Autosomal recessive spastic paraplegia type 26 Occurrence False Congenital Inferred relationship Some
Autosomal recessive spastic paraplegia type 23 Occurrence False Congenital Inferred relationship Some
Autosomal recessive spastic paraplegia type 64 Occurrence False Congenital Inferred relationship Some
Autosomal recessive spastic paraplegia type 63 Occurrence False Congenital Inferred relationship Some
Autosomal recessive spastic paraplegia type 61 Occurrence False Congenital Inferred relationship Some
Ptosis, strabismus, ectopic pupil syndrome Occurrence True Congenital Inferred relationship Some 2
Ptosis, strabismus, ectopic pupil syndrome Occurrence False Congenital Inferred relationship Some 3
Arthrogryposis hyperkeratosis syndrome lethal form Occurrence False Congenital Inferred relationship Some 4
Arthrogryposis hyperkeratosis syndrome lethal form Occurrence False Congenital Inferred relationship Some 5
Arthrogryposis hyperkeratosis syndrome lethal form Occurrence False Congenital Inferred relationship Some 6
Caudal appendage deafness syndrome Occurrence True Congenital Inferred relationship Some 4
Caudal appendage deafness syndrome Occurrence False Congenital Inferred relationship Some 5
Caudal appendage deafness syndrome Occurrence False Congenital Inferred relationship Some 6
Spastic paraplegia with Paget disease of bone syndrome Occurrence False Congenital Inferred relationship Some
Scalp defect postaxial polydactyly syndrome Occurrence True Congenital Inferred relationship Some 1
Cleft lip sequence Occurrence True Congenital Inferred relationship Some 1
Cleft uvula Occurrence False Congenital Inferred relationship Some 4
Byzanthine arch palate Occurrence True Congenital Inferred relationship Some 1
Byzanthine arch palate Occurrence False Congenital Inferred relationship Some 2
Incomplete bilateral cleft palate Occurrence False Congenital Inferred relationship Some 6
Incomplete bilateral cleft lip Occurrence True Congenital Inferred relationship Some 1
Uranostaphyloschisis Occurrence True Congenital Inferred relationship Some 1
Cleft palate with cleft lip Occurrence True Congenital Inferred relationship Some 2
Van der Woude syndrome Occurrence True Congenital Inferred relationship Some 1
Cleft lip Occurrence True Congenital Inferred relationship Some 1
Complete bilateral cleft lip Occurrence True Congenital Inferred relationship Some 1
Opitz-Frias syndrome Occurrence True Congenital Inferred relationship Some 1
Tetralogy of Fallot Occurrence True Congenital Inferred relationship Some 2
Cleft palate Occurrence True Congenital Inferred relationship Some 1
Coloboma of eye Occurrence True Congenital Inferred relationship Some 1
Thoracoceloschisis Occurrence True Congenital Inferred relationship Some 1
Thoracoceloschisis Occurrence True Congenital Inferred relationship Some 2
Coloboma of lens Occurrence False Congenital Inferred relationship Some 2
Pentalogy of Fallot Occurrence True Congenital Inferred relationship Some 3
Common atrioventricular-type ventricular septal defect Occurrence True Congenital Inferred relationship Some 1
Central cleft lip Occurrence True Congenital Inferred relationship Some 1
Bilateral incomplete cleft palate with cleft lip Occurrence False Congenital Inferred relationship Some 8
Central complete cleft palate with cleft lip Occurrence True Congenital Inferred relationship Some 2
Central incomplete cleft palate with cleft lip Occurrence True Congenital Inferred relationship Some 2
Cleft hard palate with cleft lip, bilateral Occurrence False Congenital Inferred relationship Some 6
Tetralogy of Fallot with pulmonary stenosis Occurrence True Congenital Inferred relationship Some 2
Tetralogy of Fallot with pulmonary atresia Occurrence True Congenital Inferred relationship Some 1
Dextraposition of aorta in Fallot's tetralogy Occurrence True Congenital Inferred relationship Some 3
Ventricular septal defect in Fallot's tetralogy Occurrence True Congenital Inferred relationship Some 1
Pulmonary atresia with ventricular septal defect Occurrence True Congenital Inferred relationship Some 1
Cheilopalatoschisis Occurrence False Congenital Inferred relationship Some 2

Start Previous Page 264 of 329 Next End

Reference Sets

Qualifier value foundation reference set

Back to Start