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Disease, Metabolic Bone -- See Bone Diseases, Metabolic


Diseases that affect the METABOLIC PROCESSES of BONE TISSUE 		  1
 

Disease, Mitochondrial -- See Mitochondrial Diseases


Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes 		  1
 

Disease Model, Animal -- See Disease Models, Animal


Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases 		  1
Disease models. : Toxocara : the enigmatic parasite / edited by Celia V. Holland and Huw V. Smith  2006 1
  Disease models, Animal -- 2 Related Subjects   2
Disease Models, Animal   149
Disease Models, Animals : Models of depressive disorders : psychological, biological, and genetic perspectives / edited by J. John Mann  1989 1
Disease Modesl, Animal : Recent advances on model hosts / Eleftherios Mylonakis [and others], editors  2012 1
 

Disease-Modifying Antirheumatic Drugs -- See Antirheumatic Agents


Drugs that are used to treat RHEUMATOID ARTHRITIS 		  1
 

Disease-Modifying, Antirheumatic Second-Line Drugs -- See Antirheumatic Agents


Drugs that are used to treat RHEUMATOID ARTHRITIS 		  1
 

Disease mortality -- See Mortality


All deaths reported in a given population 		  1
 

Disease, Mouth -- See Mouth Diseases


Diseases involving the MOUTH 		  1
 

Disease, Moya-Moya -- See Moyamoya Disease


A noninflammatory, progressive occlusion of the intracranial CAROTID ARTERIES and the formation of netlike collateral arteries arising from the CIRCLE OF WILLIS. Cerebral angiogram shows the puff-of-smoke (moyamoya) collaterals at the base of the brain. It is characterized by endothelial HYPERPLASIA and FIBROSIS with thickening of arterial walls. This disease primarily affects children but can also occur in adults 		  1
 

Disease, Myelodysplastic-Myeloproliferative -- See Myelodysplastic-Myeloproliferative Diseases


Clonal myeloid disorders that possess both dysplastic and proliferative features but are not properly classified as either MYELODYSPLASTIC SYNDROMES or MYELOPROLIFERATIVE DISORDERS 		  1
 

Disease, Myeloproliferative-Myelodisplastic -- See Myelodysplastic-Myeloproliferative Diseases


Clonal myeloid disorders that possess both dysplastic and proliferative features but are not properly classified as either MYELODYSPLASTIC SYNDROMES or MYELOPROLIFERATIVE DISORDERS 		  1
 

Disease, Myocardial -- See Cardiomyopathies


A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS) 		  1
 

Disease, Nail -- See Nail Diseases


Diseases of the nail plate and tissues surrounding it. The concept is limited to primates 		  1
 

Disease, Nasal -- See Nose Diseases


Disorders of the nose, general or unspecified 		  1
 

Disease, Nasopharyngeal -- See Nasopharyngeal Diseases


Pathological processes involving the NASOPHARYNX 		  1
 

Disease, Neglected -- See Neglected Diseases


Diseases that are underfunded and have low name recognition but are major burdens in less developed countries. The World Health Organization has designated six tropical infectious diseases as being neglected in industrialized countries that are endemic in many developing countries (HELMINTHIASIS; LEPROSY; LYMPHATIC FILARIASIS; ONCHOCERCIASIS; SCHISTOSOMIASIS; and TRACHOMA) 		  1
 

Disease, Neonatal -- See Infant, Newborn, Diseases


Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts 		  1
 

Disease, Nervous System -- See Nervous System Diseases


Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle 		  1
 

Disease, Neurohypophyseal -- See Pituitary Diseases


Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures 		  1
 

Disease, Neuronopathic Gaucher -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement 		  1
 

Disease, Non-Neuronopathic Gaucher -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement 		  1
 

Disease, Nose -- See Nose Diseases


Disorders of the nose, general or unspecified 		  1
 

Disease Notification -- See Also Mandatory Reporting


A legal requirement that designated types of information acquired by professionals or institutions in the course of their work be reported to appropriate authorities 		  1
Disease Notification.   7
Disease Notification -- Methods   2
 

Disease Notifications -- See Disease Notification


Notification or reporting by a physician or other health care provider of the occurrence of specified contagious diseases such as tuberculosis and HIV infections to designated public health agencies. The United States system of reporting notifiable diseases evolved from the Quarantine Act of 1878, which authorized the US Public Health Service to collect morbidity data on cholera, smallpox, and yellow fever; each state in the US has its own list of notifiable diseases and depends largely on reporting by the individual health care provider. (From Segen, Dictionary of Modern Medicine, 1992) 		  1
Disease -- nurses'instruction : Pathophysiology : the biologic basis for disease in adults and children / [edited by] Kathryn L. McCance, Sue E. Huether  1998 1
 

Disease nursing -- See Nursing Care


Care given to patients by nursing service personnel 		  1
 

Disease, Occupational -- See Occupational Diseases


Diseases caused by factors involved in one's employment 		  1
 

Disease, Ocular Paraneoplastic -- See Paraneoplastic Syndromes, Ocular


Ocular manifestations secondary to various NEOPLASMS in which antibodies to antigens of the primary tumor cross-react with ocular antigens. This autoimmune response often leads to visual loss and other ocular dysfunctions 		  1
 

Disease, Orbital -- See Orbital Diseases


Diseases of the bony orbit and contents except the eyeball 		  1
 

Disease, Orphan -- See Rare Diseases


A large group of diseases which are characterized by a low prevalence in the population. They frequently are associated with problems in diagnosis and treatment 		  1
 

Disease, Osler's -- See Telangiectasia, Hereditary Hemorrhagic


An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA 		  1
 

Disease, Otolaryngologic -- See Otorhinolaryngologic Diseases


Pathological processes of the ear, the nose, and the throat, also known as the ENT diseases 		  1
 

Disease, Otolaryngological -- See Otorhinolaryngologic Diseases


Pathological processes of the ear, the nose, and the throat, also known as the ENT diseases 		  1
 

Disease, Otologic -- See Ear Diseases


Pathological processes of the ear, the hearing, and the equilibrium system of the body 		  1
 

Disease, Otological -- See Ear Diseases


Pathological processes of the ear, the hearing, and the equilibrium system of the body 		  1
 

Disease, Otorhinolaryngologic -- See Otorhinolaryngologic Diseases


Pathological processes of the ear, the nose, and the throat, also known as the ENT diseases 		  1
 

Disease, Otorhinolaryngological -- See Otorhinolaryngologic Diseases


Pathological processes of the ear, the nose, and the throat, also known as the ENT diseases 		  1
 

Disease Outbreak -- See Disease Outbreaks


Sudden increase in the incidence of a disease. The concept includes EPIDEMICS and PANDEMICS 		  1
 

Disease Outbreak, Infectious -- See Disease Outbreaks


Sudden increase in the incidence of a disease. The concept includes EPIDEMICS and PANDEMICS 		  1
  Disease outbreaks -- 2 Related Subjects   2
Disease Outbreaks   82
Disease Outbreaks -- Congresses : Vector-borne diseases : understanding the environmental, human health, and ecological connections : workshop summary / rapporteurs, Stanley M. Lemon [and others] ; Forum on Microbial Threats, Board on Global Health, Institute of Medicine of the National Academies  2008 1
Disease Outbreaks -- economics   4
Disease Outbreaks -- ethics   4
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