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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
Neonatal candidiasis of lung Occurrence True Neonatal Inferred relationship Some 2
Neonatal systemic candidosis (disorder) Occurrence True Neonatal Inferred relationship Some 2
Neonatal candidiasis (disorder) Occurrence True Neonatal Inferred relationship Some 2
Neonatal mucocutaneous infection caused by Candida (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal oral candidiasis Occurrence True Neonatal Inferred relationship Some 1
Neonatal epistaxis (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal obstruction of nasolacrimal duct Occurrence True Neonatal Inferred relationship Some 2
Neonatal haemorrhage of kidney Occurrence True Neonatal Inferred relationship Some 1
Neonatal haemorrhage of urinary bladder Occurrence True Neonatal Inferred relationship Some 1
Neonatal hemorrhage of uterus Occurrence True Neonatal Inferred relationship Some 1
Syndrome of infant of mother with gestational diabetes Occurrence False Neonatal Inferred relationship Some 1
Neonatal hyperglycemia due to iatrogenic intravenous therapy (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal tetany without calcium deficiency Occurrence True Neonatal Inferred relationship Some 1
Neonatal tetany without magnesium deficiency (disorder) Occurrence True Neonatal Inferred relationship Some 1
Mixed neonatal apnoea Occurrence True Neonatal Inferred relationship Some 6
Mixed neonatal apnoea Occurrence True Neonatal Inferred relationship Some 8
Neonatal Marfan syndrome is a rare, severe and life-threatening genetic disease, occurring during the neonatal period, characterized by classical Marfan syndrome manifestations in addition to facial dysmorphism (megalocornea, iridodonesis, ectopia lentis, crumpled ears, loose redundant skin giving a senile facial appearance), flexion joint contractures, pulmonary emphysema, and a severe, rapidly progressive cardiovascular disease (including ascending aortic dilatation and severe mitral and/or tricuspid valve insufficiency). Additionally, skeletal manifestations (arachnodactyly, dolichostenomelia, pectus deformities) are also associated. Occurrence True Neonatal Inferred relationship Some 4
Autoimmune neonatal thrombocytopenia Occurrence True Neonatal Inferred relationship Some 2
Acquired subglottic stenosis in newborn Occurrence True Neonatal Inferred relationship Some 1
Neonatal milia (disorder) Occurrence True Neonatal Inferred relationship Some 1
Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (disorder) Occurrence True Neonatal Inferred relationship Some 1
Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (disorder) Occurrence True Neonatal Inferred relationship Some 1
Classic onset hemorrhagic disease of newborn due to vitamin K deficiency Occurrence True Neonatal Inferred relationship Some 1
Hemorrhagic disease of the newborn due to vitamin K deficiency Occurrence True Neonatal Inferred relationship Some 1
Acquired periventricular cysts of newborn Occurrence True Neonatal Inferred relationship Some 1
Hypermelanosis following phototherapy for neonatal jaundice (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal brainstem dysfunction is a rare neurologic disease characterized by the association of suction-swallowing dysfunction, abnormal laryngeal sensitivity and motility manifesting with dyspnea or obstructive apnea-hypopnea. gastroesophageal reflux (generally resistant to medication) and cardiac vagal overactivity (e.g. brachycardia, vasovagal episodes) of varying degrees of severity. Impaired social interaction has also been reported. Occurrence True Neonatal Inferred relationship Some 1
Bilateral retinopathy of prematurity Occurrence True Neonatal Inferred relationship Some 1
Bilateral retinopathy of prematurity Occurrence True Neonatal Inferred relationship Some 2
Bilateral retinopathy of prematurity of eyes stage 3 - ridge with extraretinal fibrovascular proliferation Occurrence True Neonatal Inferred relationship Some 1
Bilateral retinopathy of prematurity of eyes stage 3 - ridge with extraretinal fibrovascular proliferation Occurrence True Neonatal Inferred relationship Some 2
Retinopathy of prematurity of bilateral eyes stage 2 - intraretinal ridge (disorder) Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity of bilateral eyes stage 2 - intraretinal ridge (disorder) Occurrence True Neonatal Inferred relationship Some 2
Retinopathy of prematurity of right eye Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity of left eye stage 1 - demarcation line Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity of right eye stage 3 - ridge with extraretinal fibrovascular proliferation Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity of left eye stage 3 - ridge with extraretinal fibrovascular proliferation (disorder) Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity of right eye stage 2 - intraretinal ridge (disorder) Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity of right eye stage 1 - demarcation line (disorder) Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity of bilateral eyes stage 1 - demarcation line (disorder) Occurrence True Neonatal Inferred relationship Some 2
Retinopathy of prematurity of bilateral eyes stage 1 - demarcation line (disorder) Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity of left eye stage 2 - intraretinal ridge (disorder) Occurrence True Neonatal Inferred relationship Some 1
Retinopathy of prematurity of left eye (disorder) Occurrence True Neonatal Inferred relationship Some 1
Severe neonatal-onset encephalopathy with microcephaly is a rare monogenic disease with epilepsy characterized by neonatal-onset encephalopathy, microcephaly, severe developmental delay or absent development, breathing abnormalities (including central hypoventilation and/or respiratory insufficiency), intractable seizures, abnormal muscle tone and involuntary movements. Early death is usual. Occurrence True Neonatal Inferred relationship Some 2
Neonatal coxsackie virus syndrome Occurrence True Neonatal Inferred relationship Some 1
Tetanus neonatorum (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal colibacillosis (disorder) Occurrence True Neonatal Inferred relationship Some 1
Transitory neonatal hypernatremia Occurrence True Neonatal Inferred relationship Some 1
Transitory ileus of prematurity Occurrence True Neonatal Inferred relationship Some 1
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized blistering at birth that usually regresses within the first 6 to 24 months of life. Occurrence False Neonatal Inferred relationship Some 1
Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder) Occurrence True Neonatal Inferred relationship Some 2
Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency is a rare, hereditary, mitochondrial oxidative phosphorylation disorder characterized by severe neonatal lactic acidosis and deficiency of mitochondrial complexes I, II and III. Clinical features are variable and may include hypotonia, respiratory distress with cyanosis, failure to thrive, feeding difficulties, hypoglycemia, dehydration, vomiting, seizures, and a risk of multiple organ failure. Occurrence True Neonatal Inferred relationship Some 1
Neonatal inflammatory skin and bowel disease is a rare, life-threatening, autoinflammatory syndrome with immune deficiency disorder characterized by early-onset, life-long inflammation, affecting the skin and bowel, associated with recurrent infections. Patients present perioral and perianal psoriasiform erythema and papular eruption with pustules, failure to thrive associated with chronic malabsorptive diarrhea, intercurrent gastrointestinal infections and feeding troubles, as well as absent, short or broken hair and trichomegaly. Recurrent cutaneous and pulmonary infections lead to recurrent blepharitis, otitis externa and bronchiolitis. Occurrence True Neonatal Inferred relationship Some 1
Neonatal inflammatory skin and bowel disease is a rare, life-threatening, autoinflammatory syndrome with immune deficiency disorder characterized by early-onset, life-long inflammation, affecting the skin and bowel, associated with recurrent infections. Patients present perioral and perianal psoriasiform erythema and papular eruption with pustules, failure to thrive associated with chronic malabsorptive diarrhea, intercurrent gastrointestinal infections and feeding troubles, as well as absent, short or broken hair and trichomegaly. Recurrent cutaneous and pulmonary infections lead to recurrent blepharitis, otitis externa and bronchiolitis. Occurrence True Neonatal Inferred relationship Some 2
Hypoinsulinemic hypoglycemia and body hemihypertrophy is a rare, genetic, endocrine disease characterized by neonatal macrosomia, asymmetrical overgrowth (typically manifesting as left-sided hemihypertrophy) and recurrent, severe hypoinsulinemic (or hypoketotic hypo-fatty-acidemic) hypoglycemia in infancy, which results in episodes of reduced consciousness and seizures. Occurrence True Neonatal Inferred relationship Some 1
Sterile multifocal osteomyelitis with periostitis and pustulosis is a rare, severe, genetic autoinflammatory syndrome characterized by usually neonatal onset of generalized neutrophilic cutaneous pustulosis and severe, recurrent, multifocal, aseptic osteomyelitis with marked periostitis, typically affecting distal ribs, long bones and vertebral bodies. High levels of acute-phase reactants (with no fever associated) and onychosis are frequently observed additional features. Occurrence True Neonatal Inferred relationship Some 3
A rare secondary neonatal autoimmune disease characterized by 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 1
A rare secondary neonatal autoimmune disease characterized by generalized weakness, severe hypotonia, absent or reduced deep tendon reflexes, and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrophy in the presence of a diffuse perivascular inflammatory cell exudate is observed on muscle biopsy. Occurrence True Neonatal Inferred relationship Some 2
A rare secondary neonatal autoimmune disease characterized by generalized weakness, severe hypotonia, absent or reduced deep tendon reflexes, and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrophy in the presence of a diffuse perivascular inflammatory cell exudate is observed on muscle biopsy. Occurrence True Neonatal Inferred relationship Some 1
A rare, secondary, neonatal autoimmune disease characterized by onset of hemolytic anemia in the neonatal period associated with a positive direct antiglobulin test. Hepatosplenomegaly may be associated. Occurrence True Neonatal Inferred relationship Some 1
Neonatal antiphospholipid syndrome is a rare, secondary, neonatal autoimmune disease characterized by single or recurrent episodes of venous, arterial or mixed thrombosis in a neonate whose mother does not have antiphospholipid syndrome manifestations. Patients present positive antiphospholipid antibodies and may have additional abnormalities associated (e.g. cardiac valve disease, livedo reticularis, thrombocytopenia, nephropathy, neurological manifestations). Occurrence True Neonatal Inferred relationship Some 1
Neonatal iodine exposure is a rare endocrine disease characterized by the appearance of transient hypothyroidism, usually in preterm newborns, following long or short-term topical iodine exposure. Parenteral exposure from iodinated contrast agents may similarly alter thyroid function in term neonates. Occurrence True Neonatal Inferred relationship Some 1
KCNQ2-related epileptic encephalopathy is a severe form of neonatal epilepsy that usually manifests in newborns during the first week of life with seizures (that affect alternatively both sides of the body), often accompanied by clonic jerking or more complex motor behavior, as well as signs of encephalopathy such as diffuse hypotonia, limb spasticity, lack of visual fixation and tracking and mild to moderate intellectual deficiency. The severity can range from controlled to intractable seizures and mild/moderate to severe intellectual disability. Occurrence True Neonatal Inferred relationship Some 1
Neonatal clicking hip Occurrence True Neonatal Inferred relationship Some 1
Neonatal extracranial head trauma Occurrence False Neonatal Inferred relationship Some 1
Neonatal scalp injury Occurrence False Neonatal Inferred relationship Some 2
Neonatal bruising of scalp Occurrence False Neonatal Inferred relationship Some 2
Acquired hydrocephalus of newborn Occurrence True Neonatal Inferred relationship Some 1
Neonatal abrasion of skin of scalp (disorder) Occurrence True Neonatal Inferred relationship Some 1
Acute respiratory distress in newborn with surfactant disorder Occurrence False Neonatal Inferred relationship Some 1
Seizures complicating infection in the newborn (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal viral dacryocystitis Occurrence True Neonatal Inferred relationship Some 1
Neonatal pyogenic infection of skin (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal dacryocystitis and conjunctivitis Occurrence True Neonatal Inferred relationship Some 1
Neonatal dacryocystitis and conjunctivitis Occurrence True Neonatal Inferred relationship Some 2
Neonatal osteomyelitis of jaw Occurrence True Neonatal Inferred relationship Some 1
Neonatal osteomyelitis of jaw Occurrence True Neonatal Inferred relationship Some 2
Neonatal infective mastitis Occurrence True Neonatal Inferred relationship Some 1
Neonatal staphylococcal scalded skin syndrome (disorder) Occurrence True Neonatal Inferred relationship Some 1
Neonatal dacryocystitis Occurrence True Neonatal Inferred relationship Some 1
Neonatal meningitis Occurrence True Neonatal Inferred relationship Some 1
Transient neonatal neutropenia due to congenital viral infection Occurrence True Neonatal Inferred relationship Some 1
Transient neonatal neutropenia due to neonatal bacterial sepsis (disorder) Occurrence True Neonatal Inferred relationship Some 1
Acquired neutropenia in newborn Occurrence True Neonatal Inferred relationship Some 2
Infantile eczema Occurrence False Neonatal Inferred relationship Some 1
Neonatal breast abscess Occurrence True Neonatal Inferred relationship Some 1
Noninfective mastitis of newborn Occurrence True Neonatal Inferred relationship Some 1
Neonatal mastitis Occurrence True Neonatal Inferred relationship Some 1
Umbilical hemorrhage after birth Occurrence True Neonatal Inferred relationship Some 1
Neonatal scalp injury Occurrence True Neonatal Inferred relationship Some 1
Neonatal bruising of scalp Occurrence True Neonatal Inferred relationship Some 1
Peptic ulcer of newborn Occurrence True Neonatal Inferred relationship Some 1
Lucey-Driscoll syndrome Occurrence True Neonatal Inferred relationship Some 1
Prolonged newborn physiological jaundice Occurrence True Neonatal Inferred relationship Some 1
ictère périnatal dû à un saignement Occurrence False Neonatal Inferred relationship Some 1
Newborn physiological jaundice Occurrence True Neonatal Inferred relationship Some 1
Neonatal jaundice due to delayed conjugation from delayed development of conjugating system Occurrence True Neonatal Inferred relationship Some 1
Fetal OR neonatal jaundice from swallowed maternal blood Occurrence False Neonatal Inferred relationship Some 1
Perinataler Ikterus durch Quetschwunde Occurrence False Neonatal Inferred relationship Some 1
ictère périnatal dû à une polycythémie Occurrence False Neonatal Inferred relationship Some 1
Neonatal jaundice Occurrence True Neonatal Inferred relationship Some 1

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