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ConceptNode typeBase domainMatched membershipIdentifier
Glaucoma
An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure whi…
DisorderPathologyVisual System [curated_secondary]AMW:DIS:110087
Glaucoma, Angle-Closure
A form of glaucoma in which the intraocular pressure increases because the angle of the anterior chamber is blocked and the aqueous humor cannot drai…
DisorderPathologyVisual System [curated_secondary]AMW:DIS:110088
Glaucoma, Neovascular
A form of secondary glaucoma which develops as a consequence of another ocular disease and is attributed to the forming of new vessels in the angle o…
Vascular DisorderPathologyVisual System [curated_secondary]AMW:DIS:110089
Glaucoma, Open-Angle
Glaucoma in which the angle of the anterior chamber is open and the trabecular meshwork does not encroach on the base of the iris.
DisorderPathologyVisual System [curated_secondary]AMW:DIS:110090
Glomerulonephritis
Inflammation of the renal glomeruli (KIDNEY GLOMERULUS) that can be classified by the type of glomerular injuries including antibody deposition, comp…
Inflammatory DisorderPathologyRenal and Urinary System [role_derived]AMW:DIS:120112
Glomerulonephritis, IGA
A chronic form of glomerulonephritis characterized by deposits of predominantly IMMUNOGLOBULIN A in the mesangial area (GLOMERULAR MESANGIUM). Deposi…
Inflammatory DisorderPathologyRenal and Urinary System [curated_secondary]AMW:DIS:120113
Glomerulonephritis, Membranoproliferative
Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a th…
Inflammatory DisorderPathologyRenal and Urinary System [curated_secondary]AMW:DIS:120114
Glomerulonephritis, Membranous
A type of glomerulonephritis that is characterized by the accumulation of immune deposits (COMPLEMENT MEMBRANE ATTACK COMPLEX) on the outer aspect of…
Inflammatory DisorderPathologyRenal and Urinary System [curated_secondary]AMW:DIS:120115
Glomerulosclerosis, Focal Segmental
A clinicopathological syndrome or diagnostic term for a type of glomerular injury that has multiple causes, primary or secondary. Clinical features i…
Degenerative DisorderPathologyRenal and Urinary System [curated_secondary]AMW:DIS:120116
Glossopharyngeal Nerve Diseases
Diseases of the ninth cranial (glossopharyngeal) nerve or its nuclei in the medulla. The nerve may be injured by diseases affecting the lower brain s…
DisorderPathologyNervous System [curated_secondary]AMW:DIS:100349
Glossopharyngeal Nerve Injuries
Traumatic injuries to the GLOSSOPHARYNGEAL NERVE.
Traumatic DisorderPathologyNervous System [curated_secondary]AMW:DIS:100341
Glucose Intolerance
A pathological state in which BLOOD GLUCOSE level is less than approximately 140 mg/100 ml of PLASMA at fasting, and above approximately 200 mg/100 m…
Metabolic DisorderPathologyEndocrine System [curated_secondary]AMW:DIS:180027
Glucose Metabolism Disorders
Pathological conditions in which the BLOOD GLUCOSE cannot be maintained within the normal range, such as in HYPOGLYCEMIA and HYPERGLYCEMIA. Etiology …
Metabolic DisorderPathologyEndocrine System [curated_secondary]AMW:DIS:180018
Glucosephosphate Dehydrogenase Deficiency
A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in ery…
Congenital DisorderPathologyHematopoietic System [curated_secondary]AMW:DIS:150018
Glycogen Storage Disease Type II
An autosomal recessively inherited glycogen storage disease caused by GLUCAN 1,4-ALPHA-GLUCOSIDASE deficiency. Large amounts of GLYCOGEN accumulate i…
Congenital DisorderPathologyNervous System [curated_secondary]AMW:DIS:100094
Glycogen Storage Disease Type IIb
An X-linked dominant multisystem disorder resulting in cardiomyopathy, myopathy and INTELLECTUAL DISABILITY. It is caused by mutation in the gene enc…
Congenital DisorderPathologyNervous System [curated_secondary]AMW:DIS:100492
Glycogen Storage Disease Type VII
An autosomal recessive glycogen storage disease in which there is deficient expression of 6-phosphofructose 1-kinase in muscle (PHOSPHOFRUCTOKINASE-1…
Congenital DisorderPathologyMusculoskeletal System [curated_secondary]AMW:DIS:050266
Glycosuria
The appearance of an abnormally large amount of GLUCOSE in the urine, such as more than 500 mg/day in adults. It can be due to HYPERGLYCEMIA or genet…
Metabolic DisorderPathologyRenal and Urinary System [curated_secondary]AMW:DIS:120182
Glycosuria, Renal
An autosomal inherited disorder due to defective reabsorption of GLUCOSE by the PROXIMAL RENAL TUBULES. The urinary loss of glucose can reach beyond …
Congenital DisorderPathologyRenal and Urinary System [curated_secondary]AMW:DIS:120149
Goiter
Enlargement of the THYROID GLAND that may increase from about 20 grams to hundreds of grams in human adults. Goiter is observed in individuals with n…
Metabolic DisorderPathologyEndocrine System [curated_secondary]AMW:DIS:190028
Goiter, Endemic
A form of IODINE deficiency disorders characterized by an enlargement of the THYROID GLAND in a significantly large fraction of a POPULATION GROUP. E…
Metabolic DisorderPathologyEndocrine System [curated_secondary]AMW:DIS:190029
Goiter, Nodular
An enlarged THYROID GLAND containing multiple nodules (THYROID NODULE), usually resulting from recurrent thyroid HYPERPLASIA and involution over many…
Metabolic DisorderPathologyEndocrine System [curated_secondary]AMW:DIS:190030
Goiter, Substernal
An enlarged THYROID GLAND with at least 50% of the gland situated behind the STERNUM. It is an unusual presentation of an intrathoracic goiter. Subst…
Metabolic DisorderPathologyEndocrine System [curated_secondary]AMW:DIS:190031
Goldenhar Syndrome
Mandibulofacial dysostosis with congenital eyelid dermoids.
SyndromePathologyMusculoskeletal System [curated_secondary]AMW:DIS:050020
Gonadal Disorders
Pathological processes of the OVARIES or the TESTES.
Metabolic DisorderPathologyEndocrine System [curated_secondary]AMW:DIS:190015
Gonadal Dysgenesis
A number of syndromes with defective gonadal developments such as streak GONADS and dysgenetic testes or ovaries. The spectrum of gonadal and sexual …
Congenital DisorderPathologyReproductive System [curated_secondary]AMW:DIS:120074
Gonadal Dysgenesis, 46,XX
The 46,XX gonadal dysgenesis may be sporadic or familial. Familial XX gonadal dysgenesis is transmitted as an autosomal recessive trait and its locus…
Congenital DisorderPathologyReproductive System [curated_secondary]AMW:DIS:120065
Gonadal Dysgenesis, 46,XY
Defects in the SEX DETERMINATION PROCESS in 46, XY individuals that result in abnormal gonadal development and deficiencies in TESTOSTERONE and subse…
Congenital DisorderPathologyReproductive System [curated_secondary]AMW:DIS:120072
Gonadal Dysgenesis, Mixed
A type of defective gonadal development in patients with a wide spectrum of chromosomal mosaic variants. Their karyotypes are of partial sex chromoso…
Congenital DisorderPathologyReproductive System [curated_secondary]AMW:DIS:120075
Gout
Metabolic disorder characterized by recurrent acute arthritis, hyperuricemia and deposition of sodium urate in and around the joints, sometimes with …
Congenital DisorderPathologyMusculoskeletal System [curated_secondary]AMW:DIS:050202