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281300000: Below reference range (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
419283014 Below reference range en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
674819018 Below reference range (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
419283014 Below reference range en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
419283014 Below reference range en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
674819018 Below reference range (qualifier value) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
674819018 Below reference range (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
149241000077115 au-dessous de l'étendue de référence fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
149241000077115 au-dessous de l'étendue de référence fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Below reference range Is a Reference range comments false Inferred relationship Existential restriction modifier (core metadata concept)
Below reference range Is a Outside reference range true Inferred relationship Existential restriction modifier (core metadata concept)
Below reference range Is a Decreased true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 5
Decreased placental secretion of chorionic gonadotropin Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Urine 17 ketogenic steroid below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
High density lipoprotein below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Low density lipoprotein cholesterol below reference range Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Cholesterol/high density lipoprotein ratio below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary thrombocytopenia with early-onset myelofibrosis Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
Euglobulin clot lysis time below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
Serum total protein below reference range Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked intellectual developmental disorder Christianson type (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital generalized hypercontractile muscle stiffness syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
Oral-facial-digital syndrome with short stature and brachymesophalangia (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 5
Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Blood magnesium below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Blood glucose below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Blood urea below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Respiratory flow rate below reference range Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Decreased forced expiratory volume Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
FEV1/FVC < 70% of predicted Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Forced expiratory volume in one second/Forced vital capacity greater than 70 percent of predicted (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Forced vital capacity below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Lung function mildly obstructed Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Lung function significantly obstructed (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Chest expansion reduced Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Decreased functional residual capacity Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Decreased total lung capacity Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Decreased lung compliance Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Low ventilation-perfusion ratio Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Decreased diffusion capacity of lung Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Blood viscosity below reference range Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial steroid-resistant nephrotic syndrome with adrenal insufficiency (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
Basal metabolic rate below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Slow metabolic rate (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Urine calcium below reference level (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Urine urate below reference range Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Serum chloride below reference range Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Serum copper below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Arterial oxygen concentration below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Arterial partial pressure of carbon dioxide below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Decreased maximal voluntary ventilation (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant thrombocytopenia with platelet secretion defect Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Serum calcium below reference range Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Short stature, brachydactyly, obesity, global developmental delay syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Severe autosomal recessive macrothrombocytopenia (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Sanjad Sakati syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
A rare genetic disease characterized by multiple intestinal atresia in association with combined immunodeficiency and inflammatory bowel disease. Clinical features include widespread atresia extending from the stomach to the rectum, homogenous calcifications in the abdominal cavity, hepatic cholestasis, cirrhosis, and chronic liver failure, hypoplastic thymus, and increased susceptibility to mainly bacteria and viruses. The immunological phenotype consists of profound generalized T-cell lymphopenia and milder natural killer cell and B-cell lymphopenia, as well as low serum levels of IgG, IgA, and IgM, with elevated serum IgE. The disease is mostly fatal in infancy or childhood. Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
Short stature, advanced bone age, early-onset osteoarthritis syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 8
Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalic osteodysplastic primordial dwarfism type II (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Microcephalic osteodysplastic primordial dwarfism type II (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Progressive cerebello-cerebral atrophy (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital autosomal recessive small-platelet thrombocytopenia (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 5
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypoalphaglobulinaemia Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
Stiffness of joint of bilateral foot regions (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
L-ferritin deficiency Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare primary bone dysplasia with increased bone density characterized by slowly progressive endosteal hyperostosis and osteosclerosis exclusively of the skull base and the calvaria, resulting in entrapment and dysfunction of cranial nerves I, II, V, VII, and VIII. First symptoms often appear during the second decade of life and include disturbances in smell, vision, facial sensation and expression, hearing, and balance, as well as headaches due to increased ocular and intracranial pressure. After the fourth decade, radiological progression is minimal, although decreased intracranial volume can lead to death in severe cases. Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
A rare genetic neurological disorder characterized by infantile onset of progressive leukoencephalopathy, microcephaly, severe global developmental delay, and spasticity resulting in quadriparesis and posture deformation. Additional features include an abnormally exaggerated startle reflex, seizures, dystonia, and hypomimia or amimia, as well as progressive chest deformities and contractures of large and hyperextensibility of small joints, among others. Thin corpus callosum is a prominent feature in brain imaging, in addition to white matter abnormalities consistent with leukoencephalopathy. Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe myopia, generalized joint laxity, short stature syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Decreased estrogen level Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
QRICH1-related intellectual disability, chondrodysplasia syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare mitochondrial disease characterised by a highly variable phenotypic spectrum comprising delayed motor development, peripheral neuropathy, cataract, short stature due to growth hormone deficiency, nystagmus, sensorineural hearing loss, dysmorphic facial features, and skeletal abnormalities consistent with spondyloepimetaphyseal dysplasia. Hyperextensible joints, achalasia, and telangiectasia have also been described. Cognition is normal. Atrophy of the pituitary gland has been observed in brain imaging. Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 8
Microcephalic primordial dwarfism, insulin resistance syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcephalic primordial dwarfism, insulin resistance syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
1p35.2 microdeletion syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Complex lethal osteochondrodysplasia (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
Amniotic fluid volume below reference range Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 1
9q33.3q34.11 microdeletion syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
11q22.2q22.3 microdeletion syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
19p13.3 microduplication syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Hemoglobin E/beta thalassemia disease (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
MIRAGE syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
Placental volume below reference range (finding) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 2
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
46,XX ovarian dysgenesis, short stature syndrome (disorder) Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 3
Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4
PYCR2-related microcephaly, progressive leucoencephalopathy Has interpretation True Below reference range Inferred relationship Existential restriction modifier (core metadata concept) 4

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