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Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Domain and all descendants
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| 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 | Endocrinology [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 Disorder | Pathology | Endocrinology [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 Disorder | Pathology | Haematology [curated_secondary] | AMW:DIS:150018 |
| 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 | Metabolic Medicine [curated_secondary] | AMW:DIS:050266 |
| 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 | Nephrology [curated_secondary] | 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 | Infectious Diseases [curated_secondary] | AMW:DIS:010459 |
| 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 | Endocrinology [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 Disorder | Pathology | Endocrinology [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 Disorder | Pathology | Endocrinology [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 Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:190031 |
| Gonadal Disorders Pathological processes of the OVARIES or the TESTES. | Metabolic Disorder | Pathology | Endocrinology [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 Disorder | Pathology | Endocrinology [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 Disorder | Pathology | Endocrinology [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 Disorder | Pathology | Endocrinology [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 Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:120075 |
| Gonorrhea Acute infectious disease characterized by primary invasion of the urogenital tract. The etiologic agent, NEISSERIA GONORRHOEAE, was isolated by Neiss… | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010103 |
| Gout Metabolic disorder characterized by recurrent acute arthritis, hyperuricemia and deposition of sodium urate in and around the joints, sometimes with … | Congenital Disorder | Pathology | Metabolic Medicine [curated_secondary], Rheumatology [curated_secondary] | AMW:DIS:050202 |
| Graft Occlusion, Vascular Obstruction of flow in biological or prosthetic vascular grafts. | Vascular Disorder | Pathology | Cardiology [curated_secondary] | AMW:DIS:230201 |
| Graft vs Host Disease The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought a… | Immune Disorder | Pathology | Rheumatology [curated_secondary] | AMW:DIS:200006 |
| Gram-Negative Bacterial Infections Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010038 |
| Gram-Positive Bacterial Infections Infections caused by bacteria that retain the crystal violet stain (positive) when treated by the gram-staining method. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010142 |
| Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | Pathologic Condition | Pathology | Haematology [curated_secondary] | AMW:DIS:150156 |
| Granuloma Inguinale Anogenital ulcers caused by Calymmatobacterium granulomatis as distinguished from lymphogranuloma inguinale (see LYMPHOGRANULOMA VENEREUM) caused by … | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010070 |
| Granuloma, Laryngeal A tumor-like nodule or mass of inflammatory granulation tissue projecting into the lumen of the LARYNX. | Pathologic Condition | Pathology | Respiratory Medicine [curated_secondary] | AMW:DIS:080022 |
| Granuloma, Lethal Midline A condition that is characterized by inflammation, ulceration, and perforation of the nose and the PALATE with progressive destruction of midline fac… | Disorder | Pathology | Respiratory Medicine [curated_secondary] | AMW:DIS:080096 |
| Granuloma, Respiratory Tract Granulomatous disorders affecting one or more sites in the respiratory tract. | Pathologic Condition | Pathology | Respiratory Medicine [curated_secondary] | AMW:DIS:080021 |
| Granulomatosis with Polyangiitis A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in a… | Inflammatory Disorder | Pathology | Respiratory Medicine [curated_secondary] | AMW:DIS:080067 |
| Granulomatous Disease, Chronic A defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granulo… | Congenital Disorder | Pathology | Haematology [curated_secondary] | AMW:DIS:150127 |
| Gray Platelet Syndrome A rare, inherited platelet disorder characterized by a selective deficiency in the number and contents of platelet alpha-granules. It is associated w… | Syndrome | Pathology | Haematology [curated_secondary] | AMW:DIS:150076 |
| Haemonchiasis Infection with nematodes of the genus HAEMONCHUS, characterized by digestive abnormalities and anemia similar to that from hookworm infestation. | Infectious Disorder | Pathology | Infectious Diseases [curated_secondary] | AMW:DIS:010466 |