Terminology Service < Semantic Lookup Platform

All terms in MESHD

Label	Id	Description
Vitamin B Deficiency	D014804	[A condition due to deficiency in any member of the VITAMIN B COMPLEX. These B vitamins are water-soluble and must be obtained from the diet because they are easily lost in the urine. Unlike the lipid-soluble vitamins, they cannot be stored in the body fat.]
Bone Diseases, Infectious	D001850	[Bone diseases caused by pathogenic microorganisms.]
Infection	D007239	[Invasion of the host organism by microorganisms that can cause pathological conditions or diseases.]
Bone Diseases, Metabolic	D001851	[Diseases that affect the METABOLIC PROCESSES of BONE TISSUE.]
Metabolic Diseases	D008659	[Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed)]
Pyonephrosis	D053018	[Distention of KIDNEY with the presence of PUS and suppurative destruction of the renal parenchyma. It is often associated with renal obstruction and can lead to total or nearly total loss of renal function.]
Hydronephrosis	D006869	[Abnormal enlargement or swelling of a KIDNEY due to dilation of the KIDNEY CALICES and the KIDNEY PELVIS. It is often associated with obstruction of the URETER or chronic kidney diseases that prevents normal drainage of urine into the URINARY BLADDER.]
Bone Marrow Diseases	D001855	[Diseases involving the BONE MARROW.]
Hematologic Diseases	D006402	[Disorders of the blood and blood forming tissues.]
Hemorrhagic Fever, Ebola	D019142	[A highly fatal, acute hemorrhagic fever, clinically very similar to MARBURG VIRUS DISEASE, caused by EBOLAVIRUS, first occurring in the Sudan and adjacent northwestern (what was then) Zaire.]
Filoviridae Infections	D018702	[Infections with viruses of the family FILOVIRIDAE. The infections in humans consist of a variety of clinically similar viral hemorrhagic fevers but the natural reservoir host is unknown.]
Hemorrhagic Fevers, Viral	D006482	[A group of viral diseases of diverse etiology but having many similar clinical characteristics; increased capillary permeability, leukopenia, and thrombocytopenia are common to all. Hemorrhagic fevers are characterized by sudden onset, fever, headache, generalized myalgia, backache, conjunctivitis, and severe prostration, followed by various hemorrhagic symptoms. Hemorrhagic fever with kidney involvement is HEMORRHAGIC FEVER WITH RENAL SYNDROME.]
Tubular Sweat Gland Adenomas	D000074009	[Various tubular forms of benign tumors of the SWEAT GLAND with glandular differentiation. Common types include syringocystadenoma papilliferum of the head and neck, and hidradenoma papilliferum of the vulva area. Hidradenoma papilliferum may be derived from mammary-like glands of the vulva.]
Adenoma, Sweat Gland	D006607	[A benign neoplasm derived from epithelial cells of sweat glands. (Stedman, 25th ed)]
Acrocallosal Syndrome	D055673	[Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL ABNORMALITIES; digital malformations, and growth retardation.]
Agenesis of Corpus Callosum	D061085	[Birth defect that results in a partial or complete absence of the CORPUS CALLOSUM. It may be isolated or a part of a syndrome (e.g., AICARDI'S SYNDROME; ACROCALLOSAL SYNDROME; ANDERMANN SYNDROME; and HOLOPROSENCEPHALY). Clinical manifestations include neuromotor skill impairment and INTELLECTUAL DISABILITY of variable severity.]
Bone Neoplasms	D001859	[Tumors or cancer located in bone tissue or specific BONES.]
Neoplasms by Site	D009371	[A collective term for precoordinated organ/neoplasm headings locating neoplasms by organ, as BRAIN NEOPLASMS; DUODENAL NEOPLASMS; LIVER NEOPLASMS; etc.]
Immunoproliferative Small Intestinal Disease	D007161	[A condition that is caused by HYPERPLASIA of LYMPHOCYTES in the small intestine (INTESTINE, SMALL) and the mesenteric LYMPH NODES. These lymphocytes produce an anomalous alpha heavy chain protein. Generally, these IPSID patients have either concurrent LYMPHOMA or develop lymphoma within a few years. The disease was first described in the Mediterranean region and is characterized by malabsorption; WEIGHT LOSS; DIARRHEA; and STEATORRHEA.]
Lymphoma	D008223	[A general term for various neoplastic diseases of the lymphoid tissue.]