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)

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 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
A rare monogenic disease with characteristics of 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. Caused by mutations in the methyl-CpG binding protein 2 (MECP2) gene.	Occurrence	True	Neonatal	Inferred relationship	Some	2
Neonatal coxsackie virus syndrome	Occurrence	True	Neonatal	Inferred relationship	Some	1
Tetanus neonatorum	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
A rare hereditary mitochondrial oxidative phosphorylation disorder characterised 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, hypoglycaemia, dehydration, vomiting, seizures, and a risk of multiple organ failure.	Occurrence	True	Neonatal	Inferred relationship	Some	1
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. Presents with 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
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. Presents with 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
A rare genetic endocrine disease characterized by neonatal macrosomia, asymmetrical overgrowth (typically manifesting as left-sided hemihypertrophy) and recurrent, severe hypoinsulinemic (or hypo ketotic hypo-fatty-acidemic) hypoglycemia in infancy, which results in episodes of reduced consciousness and seizures. There is evidence the disease can be caused by heterozygous mutation in the AKT2 gene on chromosome 19q13.	Occurrence	True	Neonatal	Inferred relationship	Some	1
A rare severe genetic autoinflammatory syndrome characterised by usually neonatal onset of generalised 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. Caused by homozygous mutation in the IL1RN gene on chromosome 2q14.	Occurrence	True	Neonatal	Inferred relationship	Some	3
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	1
A very rare secondary neonatal autoimmune disease characterised by generalised 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 very rare secondary neonatal autoimmune disease characterised by generalised 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 very 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
A rare secondary neonatal autoimmune disease with characteristics of 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 (for example cardiac valve disease, livedo reticularis, thrombocytopenia, nephropathy, neurological manifestations).	Occurrence	True	Neonatal	Inferred relationship	Some	1
A rare endocrine disease with characteristics of 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
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. Caused by heterozygous mutation in the KCNQ2 gene on chromosome 20q13.	Occurrence	True	Neonatal	Inferred relationship	Some	1
Neonatal clicking hip	Occurrence	True	Neonatal	Inferred relationship	Some	1
Neonatalt ekstrakranielt hovedtraume	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 (disorder)	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 (disorder)	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
perinatal icterus forårsaget af blødning	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
Føtal eller neonatal icterus forårsaget af synkning af maternelt blod	Occurrence	False	Neonatal	Inferred relationship	Some	1
perinatal icterus forårsaget af hudlæsion	Occurrence	False	Neonatal	Inferred relationship	Some	1
perinatal icterus forårsaget af polycytæmi	Occurrence	False	Neonatal	Inferred relationship	Some	1
Neonatal jaundice	Occurrence	True	Neonatal	Inferred relationship	Some	1

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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)