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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
Gouty arthritis of left elbow Has interpretation False Above reference range Inferred relationship Some 1
Gouty arthritis of right elbow Has interpretation False Above reference range Inferred relationship Some 1
Gouty arthritis of left wrist Has interpretation False Above reference range Inferred relationship Some 1
Gouty arthritis of right wrist Has interpretation False Above reference range Inferred relationship Some 2
Chronic tophaceous gout of left foot (disorder) Has interpretation False Above reference range Inferred relationship Some 2
Chronic tophaceous gout of right foot (disorder) Has interpretation False Above reference range Inferred relationship Some 2
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. Has interpretation True Above reference range Inferred relationship Some 1
Steroid sensitive nephrotic syndrome of childhood (disorder) Has interpretation False Above reference range Inferred relationship Some 1
Nephrotic syndrome Has interpretation True Above reference range Inferred relationship Some 1
A rare primary glomerular disease characterized by the association of congenital nephrotic syndrome, early onset renal failure and ocular anomalies with microcoria and severe neurodevelopment deficits. Has interpretation True Above reference range Inferred relationship Some 3
Nephrotic syndrome with minimal change glomerulonephritis Has interpretation False Above reference range Inferred relationship Some 1
Nephrotic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic-nephritic syndrome Has interpretation True Above reference range Inferred relationship Some 1
Steroid resistant nephrotic syndrome of childhood Has interpretation True Above reference range Inferred relationship Some 1
Congenital nephrotic syndrome Has interpretation True Above reference range Inferred relationship Some 2
Familial mesangial sclerosis Has interpretation True Above reference range Inferred relationship Some 4
Nephrotic syndrome, dense deposit disease Has interpretation True Above reference range Inferred relationship Some 1
Childhood nephrotic syndrome (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome, focal and segmental glomerular lesions Has interpretation True Above reference range Inferred relationship Some 1
LAMB2-related infantile-onset nephrotic syndrome Has interpretation True Above reference range Inferred relationship Some 2
Nephrotic syndrome secondary to glomerulonephritis Has interpretation True Above reference range Inferred relationship Some 1
A rare, genetic multisystem disorder characterized by a neurodegenerative disorder associating global developmental delay, progressive microcephaly, and progressive cerebral and cerebellar atrophy with extrapyramidal involvement, progressive optic atrophy, and in many patients early-onset steroid-resistant nephrotic syndrome. Has interpretation True Above reference range Inferred relationship Some 3
Nephrotic syndrome secondary to systemic disease Has interpretation True Above reference range Inferred relationship Some 1
A rare, genetic, renal disease characterized by hereditary nephritis leading to nephrotic syndrome and end-stage renal failure associated with sensorineural hearing loss and pretibial skin blistering followed by atrophy. Other reported manifestations include bilateral lacrimal duct stenosis, dystrophic teeth and nails, bilateral cervical ribs, unilateral kidney, distal vaginal agenesis and anemia due to beta-thalassemia minor. Has interpretation True Above reference range Inferred relationship Some 2
Nephrotic syndrome co-occurrent with human immunodeficiency virus infection (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome due to type 1 diabetes mellitus Has interpretation True Above reference range Inferred relationship Some 1
Multi-drug resistant nephrotic syndrome (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome co-occurrent and due to systemic lupus erythematosus (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome, diffuse mesangial proliferative glomerulonephritis Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome with proliferative glomerulonephritis Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome with membranous glomerulonephritis Has interpretation True Above reference range Inferred relationship Some 1
Congenital nephrotic syndrome with evidence of an underlying congenital infection (e.g. syphilis, toxoplasmosis, rubella, hepatitis B). Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome with membranoproliferative glomerulonephritis Has interpretation True Above reference range Inferred relationship Some 1
Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome Has interpretation True Above reference range Inferred relationship Some 1
Steroid-sensitive nephrotic syndrome Has interpretation True Above reference range Inferred relationship Some 1
Steroid-resistant nephrotic syndrome Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome, minor glomerular abnormality Has interpretation True Above reference range Inferred relationship Some 1
Steroid-dependent nephrotic syndrome Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome, diffuse membranous glomerulonephritis Has interpretation True Above reference range Inferred relationship Some 1
Congenital nephrotic syndrome with focal glomerulosclerosis Has interpretation True Above reference range Inferred relationship Some 2
Drash syndrome Has interpretation True Above reference range Inferred relationship Some 2
Nephrotic syndrome, diffuse endocapillary proliferative glomerulonephritis Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome due to type 2 diabetes mellitus Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome, diffuse mesangiocapillary glomerulonephritis Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome in amyloidosis Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome, diffuse crescentic glomerulonephritis Has interpretation True Above reference range Inferred relationship Some 1
Finnish congenital nephrotic syndrome Has interpretation True Above reference range Inferred relationship Some 3
Nephrotic syndrome associated with another disorder Has interpretation False Above reference range Inferred relationship Some 1
A rare, hereditary nephrotic syndrome characterized by proteinuria, hypoalbuminemia, edema, and hyperlipidemia, with an absence of response to an initial trial of corticosteroids (i.e. steroid-resistant nephrotic syndrome; SRNS) and a generally complicated course. Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome due to diabetes mellitus (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome in malaria Has interpretation True Above reference range Inferred relationship Some 2
Sporadic idiopathic steroid-resistant nephrotic syndrome (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Nephrotic syndrome in polyarteritis nodosa (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Cyclic citrullinated peptide antibody measurement above reference range (finding) Has interpretation True Above reference range Inferred relationship Some 1
Leigh syndrome with nephrotic syndrome Has interpretation False Above reference range Inferred relationship Some 3
Pyoderma gangrenosum (disorder) Has interpretation False Above reference range Inferred relationship Some 3
Bancroftian filarial fever (disorder) Has interpretation True Above reference range Inferred relationship Some 2
Malayan filarial fever Has interpretation True Above reference range Inferred relationship Some 2
Eosinophilia of peritoneal fluid (finding) Has interpretation True Above reference range Inferred relationship Some 2
Frontometaphyseal dysplasia Has interpretation True Above reference range Inferred relationship Some 2
Hyperphosphatasemia with bone disease Has interpretation True Above reference range Inferred relationship Some 3
Osteomesopyknosis is a very rare benign bone disorder characterized by bone dysplasia manifested by patchy sclerosis of the axial skeleton and increased bone mineral content. Has interpretation True Above reference range Inferred relationship Some 3
Oculodento-osseous dysplasia - mild type (disorder) Has interpretation True Above reference range Inferred relationship Some 3
Pachydermoperiostosis - familial Has interpretation True Above reference range Inferred relationship Some 2
Osteopathia striata Has interpretation True Above reference range Inferred relationship Some 2
Metaphyseal dysplasia, Braun-Tinschert type is characterized by metaphyseal undermodeling with broadening of the long bones and femora with an Erlenmeyer flask appearance, expansion and bowing of the radii with severe varus deformity and flat exostoses of the long bones at the metadiaphyseal junctions. Has interpretation True Above reference range Inferred relationship Some 2
Craniometaphyseal dysplasia - severe type Has interpretation True Above reference range Inferred relationship Some 1
A rare genetic disease characterized by sclerosing dysplasia affecting the diaphyseal and metaphyseal regions of the long bones, as well as the skull and metacarpals, in association with skin changes like those seen in ichthyosis vulgaris and premature ovarian failure with bilateral hypoplasia of the ovaries. Patients present in adulthood, primarily with swelling of the extremities and occasional mild pain in the legs. Has interpretation True Above reference range Inferred relationship Some 6
Pyle metaphyseal dysplasia Has interpretation True Above reference range Inferred relationship Some 2
Craniometaphyseal dysplasia - mild type Has interpretation True Above reference range Inferred relationship Some 1
Dysplasia with increased bone density Has interpretation True Above reference range Inferred relationship Some 2
Dysplastic cortical hyperostosis Has interpretation False Above reference range Inferred relationship Some 2
Dacryocystitis and osteopoikilosis syndrome (disorder) Has interpretation True Above reference range Inferred relationship Some 3
Mixed sclerosing bone dysplasia (disorder) Has interpretation True Above reference range Inferred relationship Some 2
Oculodento-osseous dysplasia Has interpretation True Above reference range Inferred relationship Some 3
Craniodiaphyseal dysplasia Has interpretation True Above reference range Inferred relationship Some 2
Osteopathia striata with cranial sclerosis Has interpretation True Above reference range Inferred relationship Some 2
Cranio-osteoarthropathy (COA) is a form of primary hypertrophic osteoarthropathy characterized by delayed closure of the cranial sutures and fontanels, digital clubbing, arthropathy, and periostosis. Has interpretation True Above reference range Inferred relationship Some 2
Melorheostosis Has interpretation True Above reference range Inferred relationship Some 3
Oculodento-osseous dysplasia - severe type Has interpretation True Above reference range Inferred relationship Some 3
Osteosclerosis - Stanescu type Has interpretation True Above reference range Inferred relationship Some 3
Craniometaphyseal dysplasia Has interpretation True Above reference range Inferred relationship Some 3
Osteopoikilosis Has interpretation True Above reference range Inferred relationship Some 2
12q14 microdeletion syndrome is characterized by mild intellectual deficit, failure to thrive, short stature and osteopoikilosis. It has been described in four unrelated patients. The syndrome appears to be caused by a heterozygous deletion at chromosome region 12q14, which was detected in three of the four patients. The deleted region contains the LEMD3 gene: mutations in this gene have already been implicated in osteopoikilosis. Has interpretation True Above reference range Inferred relationship Some 4
Dysosteosclerosis Has interpretation True Above reference range Inferred relationship Some 2
Grant syndrome is a rare osteogenesis imperfecta-like disorder, described in two patients to date, characterized clinically by persistent wormian bones, blue sclera, mandibular hypoplasia, shallow glenoid fossa, and campomelia. There have been no further descriptions in the literature since 1986. Has interpretation True Above reference range Inferred relationship Some 2
Infantile cortical hyperostosis (disorder) Has interpretation True Above reference range Inferred relationship Some 3
Non-chronic lymphocytic leukemia monoclonal B-cell lymphocytosis (disorder) Has interpretation True Above reference range Inferred relationship Some 1
A rare, genetic coenzyme Q10 deficiency characterized by sensorineural deafness and severe, progressive nephrotic syndrome not responding to steroid treatment. Clinical manifestations include early onset proteinuria, hypoalbuminemia and edema, leading to end-stage renal disease. The renal biopsy reveals focal segmental glomerulosclerosis and diffuse mesangial sclerosis. Rarely, seizures, ataxia and dysmorphic features have been described. Has interpretation True Above reference range Inferred relationship Some 2
A rare, genetic, primary bone dysplasia with increased bone density disorder characterized by bone abnormalities, including metaphyseal plaques, osteopathia striata, marked cranial sclerosis, and sclerosis of the ribs and long bones, as well as macrocephaly, cleft palate, hearing loss, developmental delay, and facial dysmorphism (hypertelorism, prominent forehead, wide nasal bridge). Hypotonia, tracheo-/laryngomalacia, and astigmatic myopia are also associated. Has interpretation True Above reference range Inferred relationship Some 2
A rare, hereditary, hematologic disease characterized by an increase in hemoglobin, hematocrit and erythrocyte mass resulting in plethora or ruddy complexion, headache, dizziness, tinnitus and exertional dyspnea. In some cases, thrombophlebitis and arthralgia have also been reported. Has interpretation True Above reference range Inferred relationship Some 2
Maternal pyrexia in labor Has interpretation True Above reference range Inferred relationship Some 1
Acute nephrotic syndrome (disorder) Has interpretation True Above reference range Inferred relationship Some 2
Monoclonal B-cell lymphocytosis chronic lymphocytic leukaemia-type Has interpretation True Above reference range Inferred relationship Some 1
Hyperosmolar coma due to diabetes mellitus Has interpretation True Above reference range Inferred relationship Some 1
On examination - barrel chest Has interpretation False Above reference range Inferred relationship Some 2
Barrel chest Has interpretation True Above reference range Inferred relationship Some 2
Hyperphosphatasemia tarda Has interpretation True Above reference range Inferred relationship Some 2
Pyknodysostosis Has interpretation True Above reference range Inferred relationship Some 4
A rare, genetic, haematologic disease characterised by increased levels of serum haemoglobin, haematocrit and erythrocyte mass, associated with elevated or inappropriately normal erythropoietin serum levels, occurring in various members of a family and with autosomal dominant inheritance. Has interpretation True Above reference range Inferred relationship Some 2
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock. Has interpretation True Above reference range Inferred relationship Some 4

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