FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.6  |  FHIR Version n/a  User: [n/a]

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
Periodic hyperlysinemia with hyperammonemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Mesio-occlusion of teeth Occurrence False Congenital Inferred relationship Existential restriction modifier
Supernumerary roots Occurrence False Congenital Inferred relationship Existential restriction modifier
Persistent fetal uterus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital articular rigidity with myopathy Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital eventration of left crus of diaphragm Occurrence False Congenital Inferred relationship Existential restriction modifier
Crowding of teeth Occurrence False Congenital Inferred relationship Existential restriction modifier
Reticular dysgenesis with congenital aleukocytosis Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Congenital anomaly of scapula Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of humerus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of radius Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of ulna Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of femur Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of fibula Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of tibia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of calcaneus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of tarsal bone Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of metatarsal bone Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of carpal bone Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of metacarpal bone Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of rib Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of external female genitalia Occurrence False Congenital Inferred relationship Existential restriction modifier
Acquired atresia of pulmonary valve Occurrence False Congenital Inferred relationship Existential restriction modifier
Gynandromorphism syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Group chromosomal alteration Occurrence False Congenital Inferred relationship Existential restriction modifier
Chromosomal alterations of group A Occurrence False Congenital Inferred relationship Existential restriction modifier
Chromosomal alterations of group B Occurrence False Congenital Inferred relationship Existential restriction modifier
Chromosomal alterations of group C and X Occurrence False Congenital Inferred relationship Existential restriction modifier
Chromosomal alterations of group D Occurrence False Congenital Inferred relationship Existential restriction modifier
Chromosomal alterations of group E Occurrence False Congenital Inferred relationship Existential restriction modifier
Chromosomal alterations of group F Occurrence False Congenital Inferred relationship Existential restriction modifier
Chromosomal alterations of group G and Y Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of lower respiratory system Occurrence False Congenital Inferred relationship Existential restriction modifier
Accessory structure of lower respiratory tract Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital atresia of cardiac valve Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital stenosis of cardiac valve Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cleft of cardiac valve Occurrence False Congenital Inferred relationship Existential restriction modifier
Dextrorotation of heart Occurrence False Congenital Inferred relationship Existential restriction modifier
Levoatrial cardinal vein Occurrence False Congenital Inferred relationship Existential restriction modifier
Persistent dorsal mesentery Occurrence False Congenital Inferred relationship Existential restriction modifier
Mesonephric duct cyst Occurrence False Congenital Inferred relationship Existential restriction modifier
Uterus bicornis unicollis with septate vagina Occurrence False Congenital Inferred relationship Existential restriction modifier
Rudimentary uterus in male Occurrence False Congenital Inferred relationship Existential restriction modifier
Spontaneous closure of ventricular septal defect Occurrence False Congenital Inferred relationship Existential restriction modifier
Ventricular septal defect, repaired Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary methemoglobinemia, enzymatic type Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anteversion of femur Occurrence False Congenital Inferred relationship Existential restriction modifier
Disorder of cholesterol metabolism Occurrence False Congenital Inferred relationship Existential restriction modifier
Uroporphyrinuria Occurrence False Congenital Inferred relationship Existential restriction modifier
Coproporphyrinuria Occurrence False Congenital Inferred relationship Existential restriction modifier
Protoporphyrinuria Occurrence False Congenital Inferred relationship Existential restriction modifier
Tyrosinuria Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of L-lactate dehydrogenase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deficiency of D-lactate dehydrogenase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deficiency of L-lactate dehydrogenase (cytochrome) Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deficiency of xanthine oxidase Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of butyryl-CoA dehydrogenase Occurrence False Congenital Inferred relationship Existential restriction modifier 1
Deficiency of acyl-CoA dehydrogenase Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of pyrroline-2-carboxylate reductase Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of pyrroline-5-carboxylate reductase Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of dihydrofolate reductase Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of cytochrome-b>5< reductase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deficiency of reduced nicotinamide adenine dinucleotide phosphate-ferrihemoprotein reductase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deficiency of NAPH cytochrome-c>2< reductase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deficiency of guanidinoacetate methyltransferase Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deficiency of acetyl-coenzyme A acetyltransferase Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital primary adrenocortical hypofunction Occurrence False Congenital Inferred relationship Existential restriction modifier
Deficiency of adenine phosphoribosyltransferase Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital macrognathism Occurrence False Congenital Inferred relationship Existential restriction modifier
Longitudinal deficiency of metatarsal bone Occurrence False Congenital Inferred relationship Existential restriction modifier
Patent ductus arteriosus with left-to-right shunt Occurrence False Congenital Inferred relationship Existential restriction modifier
Patent ductus arteriosus with right-to-left shunt Occurrence False Congenital Inferred relationship Existential restriction modifier
Multiple malformation syndrome with senile-like appearance Occurrence False Congenital Inferred relationship Existential restriction modifier
Talocalcaneal coalition Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of perineum Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of intestinal tract Occurrence False Congenital Inferred relationship Existential restriction modifier
Cytochrome b>3< deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Erythrocytosis due to cyanotic congenital heart disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Familial erythrocytosis due to diphosphoglycerate mutase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Trifid tongue Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of skeletal bone Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of visual system Occurrence False Congenital Inferred relationship Existential restriction modifier
Cyanotic congenital heart disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Neonatal disseminated listeriosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Isologous chimera Occurrence False Congenital Inferred relationship Existential restriction modifier
Longitudinal deficiency of foot Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital portal-systemic shunt Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital extrahepatic portal-systemic shunt Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of portal vein Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital partial portal-systemic shunt Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital splenorenal shunt Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital intrahepatic portal-systemic shunt Occurrence False Congenital Inferred relationship Existential restriction modifier
Duane's syndrome, type 1 Occurrence False Congenital Inferred relationship Existential restriction modifier
Duane's syndrome, type 2 Occurrence False Congenital Inferred relationship Existential restriction modifier
Duane's syndrome, type 3 Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of central nervous system Occurrence False Congenital Inferred relationship Existential restriction modifier
Ureterocele Occurrence False Congenital Inferred relationship Existential restriction modifier
Inherited metabolic disorder of nervous system Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Dysostosis of bone of skull Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of maxilla Occurrence False Congenital Inferred relationship Existential restriction modifier

Start Previous Page 24 of 343 Next End

This concept is not in any reference sets

Back to Start