Terminology Service < Semantic Lookup Platform

All terms in MESHD

Label	Id	Description
Chlamydia Infections	D002690	[Infections with bacteria of the genus CHLAMYDIA.]
Conjunctivitis, Bacterial	D003234	[Purulent infections of the conjunctiva by several species of gram-negative, gram-positive, or acid-fast organisms. Some of the more commonly found genera causing conjunctival infections are Haemophilus, Streptococcus, Neisseria, and Chlamydia.]
Corneal Diseases	D003316	[Diseases of the cornea.]
Leukemia, Eosinophilic, Acute	D015472	[A rare acute myeloid leukemia characterized by abnormal EOSINOPHILS in the bone marrow.]
Leukemia, Promyelocytic, Acute	D015473	[An acute myeloid leukemia in which abnormal PROMYELOCYTES predominate. It is frequently associated with DISSEMINATED INTRAVASCULAR COAGULATION.]
Diabetes Insipidus, Nephrogenic	D018500	[A genetic or acquired polyuric disorder characterized by persistent hypotonic urine and HYPOKALEMIA. This condition is due to renal tubular insensitivity to VASOPRESSIN and failure to reduce urine volume. It may be the result of mutations of genes encoding VASOPRESSIN RECEPTORS or AQUAPORIN-2; KIDNEY DISEASES; adverse drug effects; or complications from PREGNANCY., X-linked congenital nephrogenic diabetes insipidus disorders occurring mostly in males and associated with V2 RECEPTOR mutations., Congenital nephrogenic diabetes insipidus associated with mutations of AQUAPORIN-2.]
Diabetes Insipidus	D003919	[A disease that is characterized by frequent urination, excretion of large amounts of dilute URINE, and excessive THIRST. Etiologies of diabetes insipidus include deficiency of antidiuretic hormone (also known as ADH or VASOPRESSIN) secreted by the NEUROHYPOPHYSIS, impaired KIDNEY response to ADH, and impaired hypothalamic regulation of thirst.]
Leukemia, Myelomonocytic, Chronic	D015477	[A myelodysplastic-myeloproliferative disease characterized by monocytosis, increased monocytes in the bone marrow, variable degrees of dysplasia, but an absence of immature granulocytes in the blood.]
Myelodysplastic-Myeloproliferative Diseases	D054437	[Clonal myeloid disorders that possess both dysplastic and proliferative features but are not properly classified as either MYELODYSPLASTIC SYNDROMES or MYELOPROLIFERATIVE DISORDERS.]
Leukemia, Myelomonocytic, Acute	D015479	[A pediatric acute myeloid leukemia involving both myeloid and monocytoid precursors. At least 20% of non-erythroid cells are of monocytic origin.]
Neck Injuries	D019838	[General or unspecified injuries to the neck. It includes injuries to the skin, muscles, and other soft tissues of the neck.]
Alkaptonuria	D000474	[An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS.]
Acne Conglobata	D000069316	[Severe and chronic form of acne characterized by large, burrowing abscesses associated with disfigurement.]
Acne Vulgaris	D000152	[A chronic disorder of the pilosebaceous apparatus associated with an increase in sebum secretion. It is characterized by open comedones (blackheads), closed comedones (whiteheads), and pustular nodules. The cause is unknown, but heredity and age are predisposing factors.]
Alkalosis, Respiratory	D000472	[A state due to excess loss of carbon dioxide from the body. (Dorland, 27th ed)]
Hyperventilation	D006985	[A pulmonary ventilation rate faster than is metabolically necessary for the exchange of gases. It is the result of an increased frequency of breathing, an increased tidal volume, or a combination of both. It causes an excess intake of oxygen and the blowing off of carbon dioxide.]
Alkalosis	D000471	[A pathological condition that removes acid or adds base to the body fluids.]
Slipped Capital Femoral Epiphyses	D060048	[A developmental deformity in which the metaphysis of the FEMUR moves proximally and anteriorly away from FEMUR HEAD (epiphysis) at the upper GROWTH PLATE. It is most common in male adolescents and is associated with a greater risk of early OSTEOARTHRITIS of the hip.]
Acid-Base Imbalance	D000137	[Disturbances in the ACID-BASE EQUILIBRIUM of the body.]
Lecithin Cholesterol Acyltransferase Deficiency	D007863	[An autosomal recessive disorder of lipoprotein metabolism caused by mutation of LECITHIN CHOLESTEROL ACYLTRANSFERASE gene. It is characterized by low HDL-cholesterol levels, and the triad of CORNEAL OPACITIES; HEMOLYTIC ANEMIA; and PROTEINURIA with renal failure.]