Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Any direct membership
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Diabetic Coma A state of unconsciousness as a complication of diabetes mellitus. It occurs in cases of extreme HYPERGLYCEMIA or extreme HYPOGLYCEMIA as a complicat… | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:190013 |
| DiGeorge Syndrome Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cel… | Syndrome | Pathology | Endocrinology [curated_secondary] | AMW:DIS:050309 |
| Disorder of Sex Development, 46,XY Congenital conditions in individuals with a male karyotype, in which the development of the gonadal or anatomical sex is atypical. | Congenital Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:120069 |
| Disorders of Sex Development In gonochoristic organisms, congenital conditions in which development of chromosomal, gonadal, or anatomical sex is atypical. Effects from exposure … | Congenital Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:120062 |
| Donohue Syndrome Rare autosomal recessive syndrome of extreme insulin resistance due to mutations in the binding domain of INSULIN RECEPTOR. Clinical features include… | Syndrome | Pathology | Endocrinology [curated_secondary] | AMW:DIS:050311 |
| Dwarfism A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is… | Congenital Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:050006 |
| Dwarfism, Pituitary A form of dwarfism caused by complete or partial GROWTH HORMONE deficiency, resulting from either the lack of GROWTH HORMONE-RELEASING FACTOR from th… | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:050011 |
| Dyslipidemias Abnormalities in the serum levels of LIPIDS, including overproduction or deficiency. Abnormal serum lipid profiles may include high total CHOLESTEROL… | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:180039 |
| Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:190001 |
| Eunuchism The state of being a eunuch, a male without TESTES or whose testes failed to develop. It is characterized by the lack of mature male GERM CELLS and T… | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:190017 |
| Euthyroid Sick Syndromes Conditions of abnormal THYROID HORMONES release in patients with apparently normal THYROID GLAND during severe systemic illness, physical TRAUMA, and… | Syndrome | Pathology | Endocrinology [curated_secondary] | AMW:DIS:190027 |
| Familial Hypophosphatemic Rickets A hereditary disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and… | Congenital Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:050080 |
| Gigantism The condition of accelerated and excessive GROWTH in children or adolescents who are exposed to excess HUMAN GROWTH HORMONE before the closure of EPI… | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:050034 |
| 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 |
| 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 |
| Hashimoto Disease Chronic autoimmune thyroiditis, characterized by the presence of high serum thyroid AUTOANTIBODIES; GOITER; and HYPOTHYROIDISM. | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:190040 |
| Hyperaldosteronism A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION … | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:190010 |
| Hyperandrogenism A condition caused by the excessive secretion of ANDROGENS from the ADRENAL CORTEX; the OVARIES; or the TESTES. The clinical significance in males is… | Congenital Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:120066 |
| Hypercholesterolemia A condition with abnormally high levels of CHOLESTEROL in the blood. It is defined as a cholesterol value exceeding the 95th percentile for the popul… | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:180041 |
| Hyperglycemia Abnormally high BLOOD GLUCOSE level. | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:180026 |
| Hyperglycemic Hyperosmolar Nonketotic Coma A serious complication of TYPE 2 DIABETES MELLITUS. It is characterized by extreme HYPERGLYCEMIA; DEHYDRATION; serum hyperosmolarity; and depressed c… | Metabolic Disorder | Pathology | Endocrinology [curated_secondary] | AMW:DIS:190014 |