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Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Base domain only
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| 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 Disorder | Pathology | Base domain | AMW:DIS:120116 |
| Glomus Jugulare Tumor A paraganglioma involving the glomus jugulare, a microscopic collection of chemoreceptor tissue in the adventitia of the bulb of the jugular vein. It… | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040300 |
| Glomus Tumor A blue-red, extremely painful vascular neoplasm involving a glomeriform arteriovenous anastomosis (glomus body), which may be found anywhere in the s… | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040447 |
| Glomus Tympanicum Tumor A rare PARAGANGLIOMA involving the GLOMUS TYMPANICUM, a collection of chemoreceptor tissue adjacent to the TYMPANIC CAVITY. It can cause TINNITUS and… | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040301 |
| Glossalgia Painful sensations in the tongue, including a sensation of burning. | Pathologic Condition | Pathology | Base domain | AMW:DIS:070083 |
| Glossitis Inflammation of the tongue. | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:070084 |
| Glossitis, Benign Migratory An idiopathic disorder of the tongue characterized by the loss of filiform papillae leaving reddened areas of circinate macules bound by a white band… | Inflammatory Disorder | Pathology | Base domain | AMW:DIS:070085 |
| 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… | Disorder | Pathology | Base domain | AMW:DIS:100349 |
| Glossopharyngeal Nerve Injuries Traumatic injuries to the GLOSSOPHARYNGEAL NERVE. | Traumatic Disorder | Pathology | Base domain | AMW:DIS:100341 |
| Glossoptosis Posterior displacement of the TONGUE toward the PHARYNX. It is often a feature in syndromes such as in PIERRE ROBIN SYNDROME and DOWN SYNDROME and as… | Disorder | Pathology | Base domain | AMW:DIS:070086 |
| Glucagonoma An almost always malignant GLUCAGON-secreting tumor derived from the PANCREATIC ALPHA CELLS. It is characterized by a distinctive migratory ERYTHEMA;… | Neoplastic Disorder | Pathology | Base domain | AMW:DIS:040369 |
| 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 Disorder | Pathology | Base domain | 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 Disorder | Pathology | Base domain | 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 Disorder | Pathology | Base domain | AMW:DIS:150018 |
| Glycogen Storage Disease A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent… | Congenital Disorder | Pathology | Base domain | AMW:DIS:160087 |
| Glycogen Storage Disease Type I An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose producti… | Congenital Disorder | Pathology | Base domain | AMW:DIS:160088 |
| 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 Disorder | Pathology | Base domain | 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 Disorder | Pathology | Base domain | AMW:DIS:100492 |
| Glycogen Storage Disease Type III An autosomal recessive metabolic disorder due to deficient expression of amylo-1,6-glucosidase (one part of the glycogen debranching enzyme system). … | Congenital Disorder | Pathology | Base domain | AMW:DIS:160089 |
| Glycogen Storage Disease Type IV An autosomal recessive metabolic disorder due to a deficiency in expression of glycogen branching enzyme 1 (alpha-1,4-glucan-6-alpha-glucosyltransfer… | Congenital Disorder | Pathology | Base domain | AMW:DIS:160090 |
| Glycogen Storage Disease Type V Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise. | Congenital Disorder | Pathology | Base domain | AMW:DIS:160091 |
| Glycogen Storage Disease Type VI A hepatic GLYCOGEN STORAGE DISEASE in which there is an apparent deficiency of hepatic phosphorylase (GLYCOGEN PHOSPHORYLASE, LIVER FORM) activity. | Congenital Disorder | Pathology | Base domain | AMW:DIS:160092 |
| 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 Disorder | Pathology | Base domain | AMW:DIS:050266 |
| Glycogen Storage Disease Type VIII An x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity. Symptoms are relatively … | Congenital Disorder | Pathology | Base domain | AMW:DIS:160060 |
| 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 Disorder | Pathology | Base domain | 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 Disorder | Pathology | Base domain | AMW:DIS:120149 |
| Gnathostomiasis Infections with nematodes of the genus GNATHOSTOMA, superfamily THELAZIOIDEA. Gnathostomiasis is a food-borne zoonosis caused by eating undercooked o… | Infectious Disorder | Pathology | Base domain | AMW:DIS:010459 |
| Goat Diseases Diseases of the domestic or wild goat of the genus Capra. | Disorder | Pathology | Base domain | AMW:DIS:220013 |
| 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 Disorder | Pathology | Base domain | 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 Disorder | Pathology | Base domain | AMW:DIS:190029 |