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281302008: Above 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
419285019 Above reference range en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
674822016 Above reference range (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Above reference range Is a Reference range comments false Inferred relationship Some
Above reference range Is a Outside reference range (qualifier value) true Inferred relationship Some
Above reference range Is a Increased true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Intestinal alkaline phosphatase above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Placental alkaline phosphatase above reference range Has interpretation True Above reference range Inferred relationship Some 1
Serum amylase (pancreatic) above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Antistreptolysin O titre above reference range Has interpretation True Above reference range Inferred relationship Some 1
Camurati-Engelmann disease (CED) is a rare, clinically variable bone dysplasia syndrome characterised by hyperostosis of the long bones, skull, spine and pelvis, associated with severe pain in the extremities, a wide-based waddling gait, joint contractures, muscle weakness and easy fatigability. Has interpretation True Above reference range Inferred relationship Some 2
A rare disorder characterised by increased bone density (predominantly diaphyseal) and aregenerative corticosteroid-sensitive anaemia. The exact prevalence is unknown. Associated with mutations in the TBXAS1 gene (which encodes thromboxane synthase). Transmitted as an autosomal recessive trait. Has interpretation True Above reference range Inferred relationship Some 4
Systemic onset juvenile chronic arthritis Has interpretation True Above reference range Inferred relationship Some 3
Adult onset Still's disease Has interpretation True Above reference range Inferred relationship Some 3
Increased renin secretion Has interpretation True Above reference range Inferred relationship Some 1
Increased renal clearance Has interpretation True Above reference range Inferred relationship Some 1
Augmented renal clearance (finding) Has interpretation True Above reference range Inferred relationship Some 3
Increased renal function Has interpretation True Above reference range Inferred relationship Some 1
A rare overgrowth syndrome associated with multiple congenital anomalies characterized by tall stature, large hands and feet with large thumbs and halluces, spatulate digits, developmental delay and facial dysmorphism. Has interpretation True Above reference range Inferred relationship Some 2
A rare overgrowth syndrome with skeletal involvement characterized by long and slim body habitus and multiple skeletal manifestations, such as scoliosis, macrodactyly of the big toes, arachnodactyly of fingers and toes, camptodactyly and clinodactyly, and progressive valgus deformities of the feet. Epimetaphyseal dysplasia, bowing of the tibiae, and dysmorphic facial features (hypertelorism, high palate, or micrognathia), as well as aortic root dilatation and umbilical hernia have also been reported. Has interpretation True Above reference range Inferred relationship Some 3
A rare overgrowth syndrome with skeletal involvement characterized by pre- or postnatal onset of overgrowth, accelerated bone age in infancy and early childhood, tall stature, bony overgrowth of the skull base, spondylar dysplasia, and undermodeling of the tubular bones. Facial dysmorphism includes mild hypertelorism, depressed nasal bridge, short and broad nose, and full lower lip. Additional reported features are scoliosis, as well as delayed puberty, cryptorchidism, and hypospadias. Has interpretation True Above reference range Inferred relationship Some 3
Serum T4 above reference range Has interpretation True Above reference range Inferred relationship Some 1
T3 uptake above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Thyroid binding globulin above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Serum female sex hormone above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Serum male sex hormone above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Free androgenic index above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Serum estradiol above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Urine norepinephrine above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Pregnanetriol above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Estriol in serum above reference range Has interpretation True Above reference range Inferred relationship Some 1
Fetoplacental hormone above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Pituitary function test above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Increased placental secretion of chorionic gonadotropin Has interpretation True Above reference range Inferred relationship Some 1
Urine adrenalin above reference range Has interpretation True Above reference range Inferred relationship Some 1
Urine 17 ketogenic steroid above reference range Has interpretation True Above reference range Inferred relationship Some 1
Lethal hydranencephaly-diaphragmatic hernia syndrome is a rare, genetic, lethal, multiple congenital anomalies syndrome characterized by hydranencephaly and diaphragmatic hernia, as well as macrocephaly, a widely open anterior fontanel, scaphoid abdomen and hypotonia. Additionally, congenital heart defects, polyhydramnios and pulmonary hypertension have also been associated. Has interpretation True Above reference range Inferred relationship Some 5
Amniotic fluid alpha-fetoprotein above reference range Has interpretation True Above reference range Inferred relationship Some 1
Euglobulin clot lysis time above reference range Has interpretation True Above reference range Inferred relationship Some 1
Free immunoglobulin light chain above reference range Has interpretation True Above reference range Inferred relationship Some 1
Plasma protein above reference range Has interpretation True Above reference range Inferred relationship Some 1
Serum protein above reference range Has interpretation False Above reference range Inferred relationship Some 1
Serum total protein above reference range Has interpretation True Above reference range Inferred relationship Some 1
Hyperfibrinolysis Has interpretation True Above reference range Inferred relationship Some 1
Antepartum haemorrhage with hyperfibrinolysis Has interpretation True Above reference range Inferred relationship Some 2
Azotemia (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Uremia Has interpretation True Above reference range Inferred relationship Some 1
Uremic neuropathy Has interpretation True Above reference range Inferred relationship Some 1
Chronic hypertensive uremia Has interpretation True Above reference range Inferred relationship Some 4
Uremic acidosis Has interpretation True Above reference range Inferred relationship Some 2
Uremia following molar AND/OR ectopic pregnancy Has interpretation False Above reference range Inferred relationship Some 6
Failed attempted abortion with uremia (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Uraemia in pregnancy without hypertension Has interpretation True Above reference range Inferred relationship Some 3
Congenital uraemia Has interpretation True Above reference range Inferred relationship Some 3
Pericarditis secondary to uremia Has interpretation True Above reference range Inferred relationship Some 4
Induced termination of pregnancy complicated by uraemia Has interpretation True Above reference range Inferred relationship Some 1
Acute pericarditis co-occurrent and due to uremia (disorder) Has interpretation True Above reference range Inferred relationship Some 5
Azotemia due to intrarenal disease (disorder) Has interpretation True Above reference range Inferred relationship Some 2
Uremia due to inadequate renal perfusion (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Postrenal azotemia (disorder) Has interpretation True Above reference range Inferred relationship Some 2
Prerenal azotemia (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Illegal abortion with uremia Has interpretation False Above reference range Inferred relationship Some 3
Legal abortion with uremia Has interpretation False Above reference range Inferred relationship Some 3
Postrenal uremia (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Abnormally increased cellular element of blood Has interpretation True Above reference range Inferred relationship Some 1
Cerebrospinal fluid cell content above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
CSF: erythrocytosis Has interpretation True Above reference range Inferred relationship Some 1
Cerebrospinal fluid lymphocytosis (finding) Has interpretation True Above reference range Inferred relationship Some 1
CSF: polymorphonuclear leukocytosis Has interpretation True Above reference range Inferred relationship Some 1
Blood magnesium above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Blood urea above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Large for gestational age newborn (finding) Has interpretation True Above reference range Inferred relationship Some 2
Whole blood folate above reference range Has interpretation True Above reference range Inferred relationship Some 1
Red blood cell folate above reference range Has interpretation True Above reference range Inferred relationship Some 1
Serum folate above reference range Has interpretation True Above reference range Inferred relationship Some 1
Respiratory flow rate above reference range Has interpretation True Above reference range Inferred relationship Some 1
Increased forced expiratory volume Has interpretation True Above reference range Inferred relationship Some 1
Lung function restrictive Has interpretation True Above reference range Inferred relationship Some 1
Chest over-expanded Has interpretation True Above reference range Inferred relationship Some 1
Increased lung compliance Has interpretation True Above reference range Inferred relationship Some 1
Increased functional residual capacity Has interpretation True Above reference range Inferred relationship Some 1
Diffusion capacity of lung above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
High ventilation-perfusion ratio (finding) Has interpretation True Above reference range Inferred relationship Some 1
Vitamin B within reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Vitamin K1 above reference range Has interpretation True Above reference range Inferred relationship Some 1
A rare disorder with multisystemic involvement and glomerulopathy characterized by progressive steroid-resistant nephrotic syndrome typically associated with focal segmental glomerulosclerosis, as well as primary adrenal insufficiency with adrenal calcifications. Age of onset and disease course are variable, with some cases presenting as severe fetal hydrops, while most patients present in infancy or early childhood and progress to end-stage renal disease within a few years. Additional features include ichthyosis, primary hypothyroidism, hypogonadism, immunodeficiency, and neurological manifestations (such as cognitive impairment, ataxia, sensorineural hearing loss, or seizures). Has interpretation True Above reference range Inferred relationship Some 3
Basal metabolic rate above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Fast metabolic rate Has interpretation True Above reference range Inferred relationship Some 1
Total iron binding capacity above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Urine calcium above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Urine urate above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Serum chloride above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Serum copper above reference range Has interpretation True Above reference range Inferred relationship Some 1
Arterial partial pressure of carbon dioxide above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Hemoglobin A1c greater than 10 percent indicating poor diabetic control (finding) Has interpretation True Above reference range Inferred relationship Some 1
Increased maximal voluntary ventilation Has interpretation True Above reference range Inferred relationship Some 1
Seizures-scoliosis-macrocephaly syndrome is a rare, genetic neurometabolic disorder characterized by seizures, macrocephaly, delayed motor milestones, moderate intellectual disability, scoliosis with no exostoses, muscular hypotonia present since birth, as well as renal dysfunction. Coarse facial features (including hypertelorism and long hypoplastic philtrum) and bilateral cryptorchidism (in males) are also commonly reported. Additional manifestations include abnormal gastrointestinal motility (resulting in constipation, diarrhea, gastroesophageal reflux and dysphagia), gait disturbances, strabismus and ventricular septal defects. Has interpretation True Above reference range Inferred relationship Some 2
A rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability, characterized by macrocephaly, intellectual disability, seizures, dysmorphic facial features (including tall forehead, downslanting palpebral fissures, hypertelorism, depressed nasal bridge, and macrostomia), megalencephaly, and small thorax. Other reported features are umbilical hernia, muscular hypotonia, global developmental delay, autistic behavior, and café-au-lait spots, among others. Has interpretation True Above reference range Inferred relationship Some 4
Complement level above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Glucoglycinuria Has interpretation True Above reference range Inferred relationship Some 2
Glucose tolerance test indicates diabetes mellitus Has interpretation True Above reference range Inferred relationship Some 1
A rare systemic disease characterized by acute or subacute onset of thrombocytopenia, anasarca (edema, pleural effusion, ascites), and systemic inflammation (fever and/or elevated C-reactive protein). Minor diagnostic categories are Castleman's disease-like features on lymph node biopsy, reticulin myelofibrosis and/or increased number of megakaryocytes in bone marrow, progressive renal insufficiency, and mild organomegaly including hepatosplenomegaly and lymphadenopathy. Most patients show elevated levels of serum alkaline phosphatase, while marked polyclonal hypergammopathy is rare. Has interpretation True Above reference range Inferred relationship Some 5
Moderately increased albuminuria due to exercise (finding) Has interpretation True Above reference range Inferred relationship Some 1
Obesity due to pituitary disease Has interpretation True Above reference range Inferred relationship Some 1
Macrocephaly-intellectual disability-left ventricular non compaction syndrome is a rare, genetic, syndromic intellectual disability characterized by motor and cognitive developmental delay with language impairment, macrocephaly, hypotonia, dysmorphic facial features (including long face, slanting palpebral fissures and prominent, flattened nose) and left ventricular noncompaction cardiomyopathy. Patients also present skeletal abnormalities (e.g. scoliosis, finger clinodactyly, pes planus), slender build and shy behavior. Strabismus and various neurological signs (including ataxia, tremor and hyperreflexia) may be associated, as well as epilepsy, autism and MRI findings showing a small cerebellum and abnormalities of the corpus callosum. A phenotypic variant with no cardiac involvement has been reported. Has interpretation True Above reference range Inferred relationship Some 3
Febrile transfusion reaction (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Grain fever Has interpretation True Above reference range Inferred relationship Some 4

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