All individuals in MESHD
Label | Id | Description |
---|---|---|
Azotemia | D053099 | [A biochemical abnormality referring to an elevation of BLOOD UREA NITROGEN and CREATININE. Azotemia can be produced by KIDNEY DISEASES or other extrarenal disorders. When azotemia becomes associated with a constellation of clinical signs, it is termed UREMIA.] |
Babesiosis | D001404 | [A group of tick-borne diseases of mammals including ZOONOSES in humans. They are caused by protozoa of the genus BABESIA, which parasitize erythrocytes, producing hemolysis. In the U.S., the organism's natural host is mice and transmission is by the deer tick IXODES SCAPULARIS.] |
Bacillaceae Infections | D016863 | [Infections with bacteria of the family BACILLACEAE.] |
Back Injuries | D019567 | [General or unspecified injuries to the posterior part of the trunk. It includes injuries to the muscles of the back.] |
Back Pain | D001416 | [Acute or chronic pain located in the posterior regions of the THORAX; LUMBOSACRAL REGION; or the adjacent regions.] |
Bacteremia | D016470 | [The presence of viable bacteria circulating in the blood. Fever, chills, tachycardia, and tachypnea are common acute manifestations of bacteremia. The majority of cases are seen in already hospitalized patients, most of whom have underlying diseases or procedures which render their bloodstreams susceptible to invasion.] |
Bacterial Infections | D001424 | [Infections by bacteria, general or unspecified.] |
Bacterial Infections and Mycoses | D001423 | [Infections caused by bacteria and fungi, general, specified, or unspecified.] |
Bacteriuria | D001437 | [The presence of bacteria in the urine which is normally bacteria-free. These bacteria are from the URINARY TRACT and are not contaminants of the surrounding tissues. Bacteriuria can be symptomatic or asymptomatic. Significant bacteriuria is an indicator of urinary tract infection.] |
Bacteroidaceae Infections | D016866 | [Infections with bacteria of the family BACTEROIDACEAE.] |
Bacteroides Infections | D001442 | [Infections with bacteria of the genus BACTEROIDES.] |
Balanitis | D001446 | [Inflammation of the head of the PENIS, glans penis.] |
Balanitis Xerotica Obliterans | D052798 | [An atrophic and sclerotic condition of the head of the PENIS, glans penis. Sometimes it leads to stenosis and occasionally obliteration of the external meatal orifice.] |
Balantidiasis | D001447 | [Infection by parasites of the genus BALANTIDIUM. The presence of Balantidium in the LARGE INTESTINE leads to DIARRHEA; DYSENTERY; and occasionally ULCER.] |
Balkan Nephropathy | D001449 | [A form of chronic interstitial nephritis that is endemic to limited areas of BULGARIA, the former YUGOSLAVIA, and ROMANIA. It is characterized by a progressive shrinking of the KIDNEYS that is often associated with uroepithelial tumors.] |
Bankart Lesions | D000070896 | [HUMERAL HEAD defect created by the sharp edge of the anterior GLENOID LABRUM as the humeral head dislocates over it., An anterior capsulolabral injury associated with a tear of the anteroinferior GLENOID LABRUM.] |
Bardet-Biedl Syndrome | D020788 | [An autosomal recessive disorder characterized by RETINITIS PIGMENTOSA; POLYDACTYLY; OBESITY; MENTAL RETARDATION; hypogenitalism; renal dysplasia; and short stature. This syndrome has been distinguished as a separate entity from LAURENCE-MOON SYNDROME. (From J Med Genet 1997 Feb;34(2):92-8)] |
Barotrauma | D001469 | [Injury following pressure changes; includes injury to the eustachian tube, ear drum, lung and stomach.] |
Barrett Esophagus | D001471 | [A condition with damage to the lining of the lower ESOPHAGUS resulting from chronic acid reflux (ESOPHAGITIS, REFLUX). Through the process of metaplasia, the squamous cells are replaced by a columnar epithelium with cells resembling those of the INTESTINE or the salmon-pink mucosa of the STOMACH. Barrett's columnar epithelium is a marker for severe reflux and precursor to ADENOCARCINOMA of the esophagus.] |
Barth Syndrome | D056889 | [Rare congenital X-linked disorder of lipid metabolism. Barth syndrome is transmitted in an X-linked recessive pattern. The syndrome is characterized by muscular weakness, growth retardation, DILATED CARDIOMYOPATHY, variable NEUTROPENIA, 3-methylglutaconic aciduria (type II) and decreases in mitochondrial CARDIOLIPIN level. Other biochemical and morphological mitochondrial abnormalities also exist.] |