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255407002: Neonatal (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
380607018 Neonatal en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
646442011 Neonatal (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
357051000195113 neonatale it Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
196371000077116 néonatal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2421001000110 Neugeborenenalter de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
17921001000119 Neonatal de Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
18541001000117 Neugeborenes de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal Is a Periods of life false Inferred relationship Some
Neonatal Is a période périnatale false Inferred relationship Some
Neonatal Is a Infancy true Inferred relationship Some
Neonatal Is a Fetal or neonatal period false Inferred relationship Some
Neonatal Is a Fetal and/or neonatal period true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hypoxic ischemic encephalopathy of newborn (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal infection of umbilicus caused by multiple microbes (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal ischaemic stroke Occurrence True Neonatal Inferred relationship Some 1
Neonatal cephalic pustulosis caused by Malassezia (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal infection of skin caused by Pseudomonas Occurrence True Neonatal Inferred relationship Some 1
Neonatal staphylococcal necrotizing fasciitis Occurrence True Neonatal Inferred relationship Some 1
Neonatal staphylococcal mastitis Occurrence True Neonatal Inferred relationship Some 1
Neonatal scald injury Occurrence True Neonatal Inferred relationship Some 1
Recurrent apnoea of newborn Occurrence True Neonatal Inferred relationship Some 1
Neonatal hyperbilirubinemia caused by substance transmitted from mother Occurrence True Neonatal Inferred relationship Some 1
Neonatal iron overload Occurrence True Neonatal Inferred relationship Some 1
Idiopathic transient neonatal hyperinsulinaemia Occurrence True Neonatal Inferred relationship Some 2
Neonatal cutis marmorata (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal diarrhoea Occurrence True Neonatal Inferred relationship Some 2
Leukemoid reaction of the newborn Occurrence True Neonatal Inferred relationship Some 2
Newborn behavior alteration (finding) Occurrence True Neonatal Inferred relationship Some 2
A type of progressive familial intrahepatic cholestasis, this disease is a severe, neonatal, hereditary disorder in bile formation that is hepatocellular in origin and not associated with extrahepatic features. Onset occurs in the neonatal period. Clinical signs of cholestasis usually appear in the first months of life with recurrent or permanent jaundice associated with hepatomegaly and severe pruritus. Patients usually develop fibrosis and end-stage liver disease before adulthood. PFIC2 is due to mutations in the ABCB11 gene (2q24) encoding the bile salt export pump (BSEP) protein resulting in impaired biliary bile acid secretion which leads to decreased bile flow and bile salt accumulation in hepatocytes with ongoing severe hepatocellular damage. Occurrence True Neonatal Inferred relationship Some 1
Neonatal glycine encephalopathy (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal toxic erythema (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal toxic erythema (disorder) Occurrence True Neonatal Inferred relationship Some 2
Progressive post haemorrhagic ventricular dilatation Occurrence True Neonatal Inferred relationship Some 2
Neonatal perforation of intestine due to congenital stenosis of intestine Occurrence True Neonatal Inferred relationship Some 1
Mild transient tachypnoea of newborn Occurrence False Neonatal Inferred relationship Some 1
Severe transient tachypnea of newborn Occurrence False Neonatal Inferred relationship Some 1
Transitory tachypnea of newborn Occurrence False Neonatal Inferred relationship Some 2
Respiratory distress syndrome in the newborn Occurrence False Neonatal Inferred relationship Some 1
Chronic pulmonary insufficiency of prematurity Occurrence False Neonatal Inferred relationship Some 1
Massive aspiration syndrome Occurrence True Neonatal Inferred relationship Some 1
Central neonatal apnea Occurrence True Neonatal Inferred relationship Some 4
Neonatal aspiration of milk Occurrence True Neonatal Inferred relationship Some 1
Neonatal aspiration of milk and regurgitated food Occurrence True Neonatal Inferred relationship Some 2
Obstructive apnea of newborn Occurrence True Neonatal Inferred relationship Some 1
Neonatal Staphylococcus aureus mastitis Occurrence True Neonatal Inferred relationship Some 1
Inflammation of breast in neonate caused by Staphylococcus epidermidis (disorder) Occurrence True Neonatal Inferred relationship Some 1
Disorder relating to short gestation AND/OR low birthweight Occurrence True Neonatal Inferred relationship Some 1
Short fetal gestation Occurrence False Neonatal Inferred relationship Some 2
An infant born before 28 completed weeks of gestation. Occurrence False Neonatal Inferred relationship Some 2
An infant born after 28 completed weeks of gestation and before 32 completed weeks of gestation. Occurrence False Neonatal Inferred relationship Some 2
Prematurity of infant (disorder) Occurrence False Neonatal Inferred relationship Some 2
An infant born after 32 completed weeks of gestation and before 37 completed weeks of gestation. Occurrence False Neonatal Inferred relationship Some 2
Complication of prematurity (disorder) Occurrence True Neonatal Inferred relationship Some 2
A rare ectodermal dysplasia syndrome characterized by neonatal teeth, trichodystrophy (with straw-like, discolored and fragile hair), onychodystrophy, and malformation of the hands and feet consisting of simian-like hands with transverse palmar creases and prominent interdigital folds, brachydactyly, and marked shortness of the first metacarpal and metatarsal bones with hypoplasia of the distal phalanges. There have been no further descriptions in the literature since 1997. Occurrence True Neonatal Inferred relationship Some 1
maladie respiratoire chronique en période périnatale Occurrence False Neonatal Inferred relationship Some 1
Perinatal pulmonary fibroplasia Occurrence False Neonatal Inferred relationship Some 1
Wilson-Mikity syndrome Occurrence False Neonatal Inferred relationship Some 1
Chronic partial asphyxia of newborn Occurrence False Neonatal Inferred relationship Some 4
Interstitial pulmonary fibrosis of prematurity Occurrence False Neonatal Inferred relationship Some 1
Pulmonary fibroplasia Occurrence True Neonatal Inferred relationship Some 1
Neonatal epilepsy due to perinatal stroke Occurrence True Neonatal Inferred relationship Some 1
Neonatal sensorineural hearing loss Occurrence True Neonatal Inferred relationship Some 3
Neonatal respiratory distress Occurrence True Neonatal Inferred relationship Some 1
A rare, genetic, syndromic intellectual disability disease characterized by severe intrauterine and post-natal growth delay, moderate to severe intellectual disability, and neonatal-onset hepatopathy with fibrosis, steatosis, and/or cholestasis, occasionally leading to liver failure. Additional variable manifestations include muscular hypotonia, zinc deficiency, recurrent infections, diabetes mellitus, joint contractures, skin and joint laxity, hypervitaminosis D, and sensorineural hearing loss. Occurrence True Neonatal Inferred relationship Some 2
A rare mitochondrial disease characterized by neonatal onset of severe cardiac and/or neurologic signs and symptoms mostly associated with a fatal outcome in the neonatal period or in infancy, although a milder phenotype with later onset and slowly progressive neurologic deterioration has also been reported. Clinical manifestations are variable and include respiratory insufficiency, hypotonia, cardiomyopathy, and seizures. Serum lactate is elevated in most cases. Brain imaging may show cerebellar atrophy or hypoplasia. Occurrence True Neonatal Inferred relationship Some 2
A rare mitochondrial disease characterized by neonatal onset of severe cardiac and/or neurologic signs and symptoms mostly associated with a fatal outcome in the neonatal period or in infancy, although a milder phenotype with later onset and slowly progressive neurologic deterioration has also been reported. Clinical manifestations are variable and include respiratory insufficiency, hypotonia, cardiomyopathy, and seizures. Serum lactate is elevated in most cases. Brain imaging may show cerebellar atrophy or hypoplasia. Occurrence True Neonatal Inferred relationship Some 3
Neonatal jaundice due to ABO incompatibility Occurrence False Neonatal Inferred relationship Some 4
Icterus neonatorum verursacht durch von der Mutter übertragene Toxine Occurrence False Neonatal Inferred relationship Some 1
Icterus neonatorum verursacht durch von der Mutter übertragene Toxine Occurrence False Neonatal Inferred relationship Some 2
Icterus neonatorum verursacht durch von der Mutter übertragene Arzneimittel Occurrence False Neonatal Inferred relationship Some 1
Icterus neonatorum verursacht durch von der Mutter übertragene Arzneimittel Occurrence False Neonatal Inferred relationship Some 2
A rare genetic neurological disorder characterized by neonatal onset of rigidity and intractable seizures, with episodic jerking already beginning in utero. Affected infants have small heads, remain visually inattentive, do not feed independently, and make no developmental progress. Frequent spontaneous apnea and bradycardia usually culminate in cardiopulmonary arrest and death in infancy, although some cases were described with a milder clinical course and survival into childhood. Occurrence True Neonatal Inferred relationship Some 1
A rare genetic neurological disorder characterized by neonatal onset of rigidity and intractable seizures, with episodic jerking already beginning in utero. Affected infants have small heads, remain visually inattentive, do not feed independently, and make no developmental progress. Frequent spontaneous apnea and bradycardia usually culminate in cardiopulmonary arrest and death in infancy, although some cases were described with a milder clinical course and survival into childhood. Occurrence True Neonatal Inferred relationship Some 2
A rare neurologic disease characterized by lethargy, hypotonia, poor feeding, opisthotonus, and a typical high-pitched cry due to bilirubin accumulation in the globus pallidus, sub-thalamic nuclei, and other brain regions, resulting from severe neonatal unconjugated hyperbilirubinemia. Onset of symptoms is typically within the first three to five days of life. Additional features include fever, apnea, seizures, and coma. Respiratory failure or refractory seizures may lead to a fatal outcome. Occurrence True Neonatal Inferred relationship Some 1
A rare neurologic disease characterized by the chronic consequences of bilirubin toxicity in the globus pallidus, sub-thalamic nuclei, and other brain regions, after exposure to high levels of unconjugated bilirubin in the neonatal period. Symptoms begin after the acute phase of bilirubin encephalopathy in the first year of life, evolve slowly over several years, and include mild to severe extrapyramidal disturbances (especially dystonia and athetosis), auditory neuropathy spectrum disorder, and oculomotor and dental abnormalities. Occurrence True Neonatal Inferred relationship Some 1
Isolated neonatal sclerosing cholangitis is a rare, genetic, biliary tract disease characterized by severe neonatal-onset cholangiopathy with patent bile ducts and absence of ichthyosiform skin lesions. Patients present with jaundice, acholic stools, hepatosplenomegaly and high serum gamma-glutamyltransferase activity. Liver histology shows portal fibrosis, ductular proliferation, hepatocellular metallothionein deposits, and intralobular bile-pigment accumulations. Some patients may also have renal disease. Occurrence True Neonatal Inferred relationship Some 1
A rare genetic neurometabolic disease characterized by early neonatal refractory seizures, hypotonia, and respiratory failure. Brain imaging reveals simplified gyral pattern of the frontal lobes, white matter abnormalities, gliosis and volume loss in various brain regions, and vasogenic edema. Serum glutamine levels are significantly elevated. Death occurs within weeks after birth. Occurrence True Neonatal Inferred relationship Some 1
A rare organic aciduria characterized by neonatal onset of hypotonia, recurrent apneic episodes, lack of psychomotor development, feeding difficulties, extrapyramidal signs, and seizures. Other reported features include microcephaly, sensorineural deafness, bradycardia, and neutropenia. Laboratory studies show increased serum lactate and urinary excretion of 3-methylglutaconic acid. Brain imaging may reveal progressive cerebral atrophy. The disease is lethal in infancy. Occurrence True Neonatal Inferred relationship Some 1
A rare, genetic, autosomal recessive axonal hereditary motor and sensory neuropathy disease characterized by prenatal onset of a severe sensorimotor axonal polyneuropathy (reflected by reduced fetal movement and polyhydramnios), manifesting, at birth, with respiratory failure requiring mechanical ventilation, profound muscular hypotonia, rapidly progressing distal muscle weakness, and absent deep tendon reflexes, in the absence of contractures, leading to death before 8 months of age. Neuropathological findings show severe loss of large- and medium-sized myelinated fibers without signs of demyelination. Occurrence True Neonatal Inferred relationship Some 2
A rare systemic condition affecting neonates born at less than 37 weeks gestational age and characterized by life-threatening organ dysfunction caused by a dysregulated host response to an infection, which may have been acquired shortly before or during birth (resulting in early-onset neonatal sepsis during the first 72 hours of life), or after birth (leading to late-onset neonatal sepsis between 72 hours and three months). Prematurity constitutes one of the primary risk factors for neonatal sepsis. The clinical picture may develop gradually with signs and symptoms like irritability, lethargy, or poor feeding, or progress rapidly to respiratory distress, fever, hypothermia, hypotension, shock, and multiple organ failure. Occurrence True Neonatal Inferred relationship Some 1
Neonatal ecthyma gangrenosum (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to umbilical cord disorder (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to injury of umbilical cord Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to entanglement of cord Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to compression of umbilical cord (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to true knot of umbilical cord Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to long umbilical cord (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to short umbilical cord Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to thrombosis of umbilical cord Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to torsion of umbilical cord Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to umbilical cord around neck (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to varices of umbilical cord (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to vasa previa of umbilical cord Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to velamentous insertion of umbilical cord (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal aspiration of amniotic fluid Occurrence True Neonatal Inferred relationship Some 1
Baby premature at delivery less than 32 weeks (finding) Occurrence True Neonatal Inferred relationship Some 2
Complication of neonatal circumcision (disorder) Occurrence True Neonatal Inferred relationship Some 1
A rare genetic disease characterized by congenital cataract, neonatal hepatic failure and cholestatic jaundice, and global developmental delay. Neonatal death due to progressive liver failure has been reported. Occurrence True Neonatal Inferred relationship Some 2
Neonatal ecchymoses (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal extradural intracranial hemorrhage (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal nontraumatic intracranial subdural hemorrhage Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by substance transmitted via breast milk Occurrence True Neonatal Inferred relationship Some 1
Neonatal effect of anti-infective agent transmitted via breast milk (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by antibacterial transmitted via breast milk (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by diethylstilbestrol transmitted via breast milk (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by hallucinogenic agent transmitted via breast milk Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by narcotic transmitted via breast milk Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by immune serum transmitted via breast milk (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder due to maternal exposure to environmental chemical via breast milk (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by nutritional substance via breast milk Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by toxic substance transmitted breast milk Occurrence False Neonatal Inferred relationship Some 1
Neonatal disorder caused by medicinal agent transmitted via breast milk (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by antineoplastic agent transmitted via breast milk Occurrence True Neonatal Inferred relationship Some 1

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