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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
2235971000005113 Neonatal da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


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 Perinatalperiode 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
Neonatal disorder caused by antineoplastic agent transmitted via breast milk Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by hypoglycemic agent via breast milk (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by endocrine agent via breast milk (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by anticonvulsant via breast milk Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by anticoagulant in breast milk Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by uterine depressor via breast milk Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by maternal analgesia transmitted via breast milk Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by maternal tobacco consumption (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal disorder caused by maternal antihypertensive medication via breast milk Occurrence True Neonatal Inferred relationship Some 1
Necrotising enterocolitis of newborn, stage 1A Occurrence True Neonatal Inferred relationship Some 1
Necrotising enterocolitis of newborn, stage 1A Occurrence True Neonatal Inferred relationship Some 2
Necrotizing enterocolitis of newborn stage 1B Bell's classification (disorder) Occurrence True Neonatal Inferred relationship Some 1
Necrotizing enterocolitis of newborn stage 1B Bell's classification (disorder) Occurrence True Neonatal Inferred relationship Some 2
Necrotising enterocolitis of newborn, Stage 2A Occurrence True Neonatal Inferred relationship Some 1
Necrotising enterocolitis of newborn, Stage 2A Occurrence True Neonatal Inferred relationship Some 2
Necrotising enterocolitis of newborn, Stage 2B Occurrence True Neonatal Inferred relationship Some 1
Necrotising enterocolitis of newborn, Stage 2B Occurrence True Neonatal Inferred relationship Some 2
Necrotizing enterocolitis of newborn stage 3A Bell's classification (disorder) Occurrence True Neonatal Inferred relationship Some 1
Necrotizing enterocolitis of newborn stage 3A Bell's classification (disorder) Occurrence True Neonatal Inferred relationship Some 2
Necrotising enterocolitis of newborn, Stage 3B Occurrence True Neonatal Inferred relationship Some 1
Necrotising enterocolitis of newborn, Stage 3B Occurrence True Neonatal Inferred relationship Some 2
A very rare secondary neonatal autoimmune disease with characteristics of neonatal-onset of erythematous skin lesions with a linear appearance that gradually become indurated and hyperpigmented and progressively present skin atrophy. Positive serum antibodies (in particular antinuclear antibodies and/or rheumatoid factor) may be associated. Occurrence True Neonatal Inferred relationship Some 2
Term infant 38 weeks Occurrence True Neonatal Inferred relationship Some 1
Term infant 37 weeks (finding) Occurrence True Neonatal Inferred relationship Some 1
Term infant 39 weeks (finding) Occurrence True Neonatal Inferred relationship Some 1
A rare genetic disease characterized by the association of Fanconi syndrome and nephrocalcinosis in addition to neonatal hyperinsulinism and macrosomia. Patients display a phenotype of proximal tubulopathy characterized by generalized aminoaciduria, low molecular weight proteinuria, glycosuria, hyperphosphaturia and hypouricemia, and additional features not normally seen in Fanconi syndrome (apart from nephrocalcinosis), namely renal impairment, hypercalciuria with relative hypocalcemia, and hypermagnesemia. Occurrence True Neonatal Inferred relationship Some 2
Neonatal jaundice due to delayed conjugation from breast milk inhibitor Occurrence True Neonatal Inferred relationship Some 1
Neonatal tuberculosis (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal transient metabolic disturbance (disorder) Occurrence True Neonatal Inferred relationship Some 1
Risk factor - been on SCBU Occurrence True Neonatal Inferred relationship Some 2
Acute aseptic myocarditis of the newborn Occurrence True Neonatal Inferred relationship Some 2
Non-traumatic intraventricular hemorrhage grade 1 during neonatal period (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal infection of skin caused by Candida Occurrence True Neonatal Inferred relationship Some 1
Non-traumatic intraventricular haemorrhage grade 2 during neonatal period Occurrence True Neonatal Inferred relationship Some 1
Non-traumatic intraventricular hemorrhage grade 3 during neonatal period (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal jaundice caused by substance transmitted via breast milk (finding) Occurrence True Neonatal Inferred relationship Some 1
Neonatal jaundice caused by substance transmitted via breast milk (finding) Occurrence False Neonatal Inferred relationship Some 2
Repair of neonatal diaphragmatic hernia Occurrence True Neonatal Inferred relationship Some 1
Neonatal jaundice due to Gilbert's syndrome (finding) Occurrence True Neonatal Inferred relationship Some 1
Snuffles in newborn Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of predominant automatisms, defined as more or less coordinated motor activity with electrographic correlate, that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of abnormal motor and/or non-motor phenomenon with electrographic correlate, or a neonatal electrographic-only seizure (without clinical correlate) that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of abnormal motor and/or non-motor phenomenon with electrographic correlate that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
An electrographic change defined by a sudden repetitive, evolving, stereotyped waveform with a beginning and end without clinical correlate that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of abnormal predominantly non-motor phenomenon with electrographic correlate that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of abnormal predominantly motor phenomenon with electrographic correlate that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of abnormal motor, non-motor or electrographic-only phenomenon occurring in sequence within a single seizure. No predominant feature can be determined instead the seizure presents with a variety of clinical signs. Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of brief (less than 100 milliseconds) involuntary single or multiple contraction(s) of muscles(s) or muscle groups of variable topography (axial, proximal limb, distal) with electrographic correlate, that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of sustained increase in muscle contraction lasting a few seconds to minutes, with electrographic correlate, that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of regularly repetitive jerking of the same muscle groups which is either symmetric or asymmetric with electrographic correlate, that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of flexion, extension, or mixed extension-flexion of predominantly proximal and truncal muscles, with electrographic correlate, that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of distinct alteration of autonomic nervous system function involving cardiovascular, pupillary, gastrointestinal, sudomotor (sweating), vasomotor, or thermoregulatory functions with electrographic correlate, that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
A sudden paroxysm of a predominant arrest (pause) of activities, freezing and immobilization with electrographic correlate, that occurs during the period from birth until 44 weeks postmenstrual age. Occurrence True Neonatal Inferred relationship Some 1
Seizures complicating intracranial hemorrhage in the newborn (disorder) Occurrence True Neonatal Inferred relationship Some 2
Neonatal jaundice due to congenital obstruction of bile duct Occurrence True Neonatal Inferred relationship Some 1
Neonatal jaundice due to swallowed maternal blood (finding) Occurrence True Neonatal Inferred relationship Some 1
Neonatal jaundice due to bruising (finding) Occurrence True Neonatal Inferred relationship Some 1
Neonatal jaundice due to inspissated bile syndrome Occurrence True Neonatal Inferred relationship Some 1
Circumcision by clamp procedure on newborn Occurrence True Neonatal Inferred relationship Some 1
Phototherapy of newborn Occurrence True Neonatal Inferred relationship Some 1
Neonatal conjunctivitis of right eye caused by Neisseria gonorrhoeae (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal conjunctivitis of left eye caused by Neisseria gonorrhoeae (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal conjunctivitis of bilateral eyes caused by Neisseria gonorrhoeae (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal conjunctivitis of bilateral eyes caused by Neisseria gonorrhoeae (disorder) Occurrence True Neonatal Inferred relationship Some 2
Newborn slipped umbilical ligature Occurrence True Neonatal Inferred relationship Some 1
Delayed separation of umbilical cord (disorder) Occurrence True Neonatal Inferred relationship Some 1
A type of self-limited focal epilepsy with onset typically between day two and seven of life. Seizures are focal tonic at onset, affecting the head, face, and limbs. Focal clonic or tonic seizures may evolve to bilateral tonic or clonic seizures. Onset may alternate between hemispheres. Autonomic features (apnea and cyanosis) are present in one third of seizures and may be the predominant manifestation. Seizure semiology may progress in a sequential pattern with tonic, clonic, myoclonic and autonomic features following each other without a single predominant feature. Clusters of seizures may occur over hours or days with the neonate behaving normally between events. Developmental progress is usually normal. The electroencephalogram (EEG) background is normal or has minor nonspecific abnormalities. Focal interictal epileptiform abnormalities can be seen in the central, centrotemporal or frontotemporal regions. MRI is normal or has nonspecific findings. Pathogenic variants are seen in KCNQ2, KCNQ3 and SCN2A. Occurrence True Neonatal Inferred relationship Some 2
A rare, genetic, neonatal diabetes mellitus syndrome, that is a variant of DEND syndrome and has clinical characteristics of neonatal insulin-dependent diabetes mellitus, mild motor, speech or cognitive delay, and the absence of epilepsy. Occurrence True Neonatal Inferred relationship Some 1
DEND syndrome is a very rare, generally severe form of neonatal diabetes mellitus characterized by a triad of developmental delay, epilepsy, and neonatal diabetes. Occurrence True Neonatal Inferred relationship Some 1
Neonatal botulism (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal aspiration pneumonitis Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity stage 5 of left eye (disorder) Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity stage 5 of right eye (disorder) Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity stage 5 of bilateral eyes (disorder) Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity stage 5 of bilateral eyes (disorder) Occurrence True Neonatal Inferred relationship Some 2
Glucose-galactose malabsorption Occurrence True Neonatal Inferred relationship Some 1
Neonatal innocent cardiac murmur (finding) Occurrence True Neonatal Inferred relationship Some 3
Rickets due to prematurity Occurrence True Neonatal Inferred relationship Some 2
Osteopenia of prematurity Occurrence True Neonatal Inferred relationship Some 1
Rumination in newborn Occurrence True Neonatal Inferred relationship Some 1

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