Terminology Service < Semantic Lookup Platform

All terms in MESHD

Label	Id	Description
Toxascariasis	D017227	[Infections with nematodes of the genus TOXASCARIS.]
Chlamydial Pneumonia	D061387	[Pneumonia caused by infections with the genus CHLAMYDIA; and CHLAMYDOPHILA, usually with CHLAMYDOPHILA PNEUMONIAE.]
Pneumonia, Bacterial	D018410	[Inflammation of the lung parenchyma that is caused by bacterial infections.]
Chlamydophila Infections	D023521	[Infections with bacteria of the genus CHLAMYDOPHILA.]
Enterobiasis	D017229	[Infection with nematodes of the genus ENTEROBIUS; E. vermicularis, the pinworm of man, causes a crawling sensation and pruritus. This condition results in scratching the area, occasionally causing scarification.]
Oxyuriasis	D010123	[Infection with nematodes of the superfamily OXYUROIDEA.]
Raynaud Disease	D011928	[An idiopathic vascular disorder characterized by bilateral Raynaud phenomenon, the abrupt onset of digital paleness or CYANOSIS in response to cold exposure or stress.]
Feline Panleukopenia	D005254	[A highly contagious DNA virus infection of the cat family, characterized by fever, enteritis and bone marrow changes. It is also called feline ataxia, feline agranulocytosis, feline infectious enteritis, cat fever, cat plague, and show fever. It is caused by FELINE PANLEUKOPENIA VIRUS or the closely related MINK ENTERITIS VIRUS or CANINE PARVOVIRUS.]
Felty Syndrome	D005258	[A rare complication of rheumatoid arthritis with autoimmune NEUTROPENIA; and SPLENOMEGALY.]
Mitochondrial Myopathies	D017240	[A group of muscle diseases associated with abnormal mitochondria function.]
Nocardia Infections	D009617	[Infections with bacteria of the genus NOCARDIA.]
Actinomycetales Infections	D000193	[Infections with bacteria of the order ACTINOMYCETALES.]
Albuminuria	D000419	[The presence of albumin in the urine, an indicator of KIDNEY DISEASES.]
Proteinuria	D011507	[The presence of proteins in the urine, an indicator of KIDNEY DISEASES.]
Microvascular Rarefaction	D000073436	[The reduction in density of the MICROVASCULATURE.]
MELAS Syndrome	D017241	[A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117)]
Mitochondrial Encephalomyopathies	D017237	[A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)]
Cerebral Small Vessel Diseases	D059345	[Pathological processes or diseases where cerebral MICROVESSELS show abnormalities. They are often associated with aging, hypertension and risk factors for lacunar infarcts (see LACUNAR INFARCTION); LEUKOARAIOSIS; and CEREBRAL HEMORRHAGE.]
alpha 1-Antitrypsin Deficiency	D019896	[Deficiency of the protease inhibitor ALPHA 1-ANTITRYPSIN that manifests primarily as PULMONARY EMPHYSEMA and LIVER CIRRHOSIS.]
Subcutaneous Emphysema	D013352	[Presence of air or gas in the subcutaneous tissues of the body.]