disease
The definitions used in this glossary of terminology either have been provided by the authors of the articles, or have been extracted wholly or in part, or paraphrased from the following sources: The American Medical Association Encyclopedia of Medicine, Charles B. Clayman, MD, Medical Editor, Random House, New York, 1989; Biotechnology from A to Z, 2d Edition, William Bains, Oxford University Press, New York, New York, 2002; A Dictionary of Genetics, 6th Edition, Robert C. King and William D. Stansfield, Oxford University Press, New York, New York, 2002; Dorland's Illustrated Medical Dictionary, 29th and 30th Editions, W. B. Saunders Company, Philadelphia, 2000, 2003; Genes VII, Benjamin Lewin, Oxford University Press, New York, New York, 2000; The Gale Encyclopedia of Genetic Disorders, Volumes I and II, Stacey L. Blachford, Ed., Thomson Learning, New York, New York, 2002; The Merriam-Webster Dictionary, Merriam-Webster, Inc., Springfield, Massachusetts, 1997; Molecular Biology of the Cell, 3rd Edition, Bruce Alberts, et al., Garland Publishing, 1994; The Random House Dictionary of the English Language, Unabridged Edition, 1966; Webster's Ninth New Collegiate Dictionary, 1991.
DEFINITION:
- disease
Used in 80 Article abstracts
Used in 80 Article abstracts
- A Case of Nephrogenic Diabetes Insipidus Caused by Obstructive Uropathy Due to Prostate Cancer
- A Low-Affinity Vasopressin V2-Receptor Gene in a Kindred with X-Linked Nephrogenic Diabetes Insipidus
- A Novel Mechanism in Recessive Nephrogenic Diabetes Insipidus: Wild-Type Aquaporin-2 Rescues the Apical Membrane Expression of Intracellularly Retained AQP2-P262L
- A Novel Polymorphism in the Coding Region of the Vasopressin Type 2 Receptor Gene
- Aminoglycoside-Mediated Rescue of a Disease-Causing Nonsense Mutation in the V2 Vasopressin Receptor Gene In Vitro and In Vivo
- An Impaired Routing of Wild-type Aquaporin-2 after Tetramerization with an Aquaporin-2 Mutant Explains Dominant Nephrogenic Diabetes Insipidus
- Aquaporin Molecular Biology and Clinical Abnormalities of the Water Transport Channels
- Autosomal Recessive Nephrogenic Diabetes Insipidus Caused by an Aquaporin-2 Mutation
- Cell-Biologic and Functional Analyses of Five New Aquaporin-2 Missense Mutations that Cause Recessive Nephrogenic Diabetes Insipidus
- Characterization of an Aquaporin-2 Water Channel Gene Mutation Causing Partial Nephrogenic Diabetes Insipidus in a Mexican Family: Evidence of Increased Frequency of the Mutation in the Town of Origin
- Clinical Characteristics of Eight Patients with Congenital Nephrogenic Diabetes Insipidus
- Clinical Presentation and Follow-Up of 30 Patients with Congenital Nephrogenic Diabetes Insipidus
- Clinical Utility of Direct Mutation Testing for Congenital Nephrogenic Diabetes Insipidus in Families
- Cognitive and Psychosocial Functioning of Patients with Congenital Nephrogenic Diabetes Insipidus
- Defective processing and trafficking of water channels in nephrogenic diabetes insipidus.
- Defects of G Protein-Coupled Signal Transduction in Human Disease
- Discovery of Aquaporins: a Breakthrough in Research on Renal Water Transport
- Disease-Causing V2 Vasopressin Receptors are Retained in Different Compartments of the Early Secretory Pathway
- Diversity of Nephrogenic Diabetes Insipidus Mutations and Importance of Early Recognition and Treatment
- Early Onset Bilateral Calcifications and Epilepsy
- Evaluation and Management of Diabetes Insipidus
- Evidence for Stabilization of Aquaporin-2 Folding Mutants by N-linked Glycosylation in the Endoplasmic Reticulum
- Functional Analysis of Aquaporin-2 Mutants Associated with Nephrogenic Diabetes Insipidus by Yeast Expression
- Functional Studies of Twelve Mutant V2 Vasopressin Receptors Related to Nephrogenic Diabetes Insipidus: Molecular Basis of a Mild Clinical Phenotype
- Hemodynamic and Coagulation Responses to 1-desamino[8-D-arginine] Vasopressin in Patients with Congenital Nephrogenic Diabetes Insipidus
- Heteroligomerization of an Aquaporin-2 Mutant with Wild-Type Aquaporin-2 and Their Misrouting to Late Endosomes/Lysosomes Explains Dominant Nephrogenic Diabetes Insipidus
- Hyponatremia and Hypernatremia
- Identification and Characterization of Aquaporin-2 Water Channel Mutations Causing Nephrogenic Diabetes Insipidus with Partial Vasopressin Response
- Importance of Aquaporin-2 Expression Levels in Genotype -Phenotype Studies in Nephrogenic Diabetes Insipidus
- Inheritance of Mutations in the V2 Receptor Gene in Thirteen Families with Nephrogenic Diabetes Insipidus
- Inherited Diseases of the Kidney
- Investigation of Folding and Degradation of In Vitro Synthesized Mutant Proteins in Microsomes
- Lithium Nephrotoxicity: A Progressive Combined Glomerular and Tubulointerstitial Nephropathy
- Lithiumogenic Disorders of the Thyroid and Parathyroid Glands as Surgical Disease
- Meniere's Disease in Congenital Nephrogenic Diabetes Insipidus: Report of Two Twins
- Methyl-β-Cyclodextrin Induces Vasopressin-Independent Apical Accumulation of Aquaporin-2 in the Isolated, Perfused Rat Kidney
- Molecular Analyses of the Vasopressin Type 2 Receptor and Aquaporin-2 Genes in Brazilian Kindreds with Nephrogenic Diabetes Insipidus
- Molecular Genetic Study of Congenital Nephrogenic Diabetes Insipidus and Rescue of Mutant Vasopressin V2 Receptor by Chemical Chaperones
- Molecular and Cellular Defects in Nephrogenic Diabetes Insipidus
- Mutations and Diseases of G Protein Coupled Receptors
- Mutations in the V2 Vasopressin Receptor Gene are Associated with X-linked Nephrogenic Diabetes Insipidus
- Mutations in the Vasopressin V2 Receptor Gene in Families with Nephrogenic Diabetes Insipidus and Functional Expression of the Q-2 Mutant
- Mutations in the Vasopressin V2 Receptor and Aquaporin-2 Genes in 12 Families with Congenital Nephrogenic Diabetes Insipidus
- Nature and Recurrence of AVPR2 Mutations in X-Linked Nephrogenic Diabetes Insipidus
- Neonatal Mortality in an Aquaporin-2 Knock-in Mouse Model of Recessive Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus (Bichet - November 1998)
- Nephrogenic Diabetes Insipidus--Prodromal Phase of Multiple Myeloma
- Nephrogenic Diabetes Insipidus. A Personal Perspective
- Nephrogenic Diabetes Insipidus. A V2 Vasopressin Receptor Unable to Stimulate Adenylyl Cyclase
- Nephrogenic Diabetes Insipidus: An X Chromosome-Linked Dominant Inheritance Pattern with a Vasopressin Type 2 Receptor Gene that is Structurally Normal
- Nephrogenic Diabetes Insipidus: Clinical Symptoms, Pathogenesis, Genetics and Treatment
- Nephrogenic Diabetes Insipidus: Close Linkage with Markers from the Distal Long Arm of the Human X Chromosome
- Nephrogenic Diabetes Insipidus: Identification of the Genetic Defect
- Nephrogenic diabetes insipidus.
- Novel Vasopressin Type 2 (AVPR2) Gene Mutations in Brazilian Nephrogenic Diabetes Insipidus Patients
- Pathogenesis and Treatment of Autosomal-Dominant Nephrogenic Diabetes Insipidus Caused by an Aquaporin 2 Mutation
- Pathophysiology of the Aquaporin Water Channels
- Pharmacological Chaperones in Nephrogenic Diabetes Insipidus: Possibilities for Clinical Application
- Report of 33 Novel AVPR2 Mutations and Analysis of 117 Families with X-Linked Nephrogenic Diabetes Insipidus
- Rescue of a Nephrogenic Diabetes Insipidus-Causing Vasopressin V2 Receptor Mutant by Cell-Penetrating Peptides
- Reversed Polarized Delivery of an Aquaporin-2 Mutant Causes Dominant Nephrogenic Diabetes Insipidus
- Role of Aquaporin Water Channels in Kidney and Lung
- Routing of the aquaporin-2 water channel in health and disease.
- Six Novel Mutations in the Vasopressin V2 Receptor Gene Causing Nephrogenic Diabetes Insipidus
- The Aquaporin Family of Water Channel Proteins in Clinical Medicine
- The Aquaporins. A Family of Water Channel Proteins
- The Molecular Basis of Nephrogenic Diabetes Insipidus
- Two Novel Mutations in the Vasopressin V2 Receptor Gene in Patients with Congenital Nephrogenic Diabetes Insipidus
- V2R Structure and Diabetes Insipidus
- Vasopressin Receptor Mutations Causing Nephrogenic Diabetes Insipidus
- Vasopressin Type-2 Receptor and Aquaporin-2 Water Channel Mutants in Nephrogenic Diabetes Insipidus
- Water Transport Across Mammalian Cell Membranes
- X-Linked Nephrogenic Diabetes Insipidus Mutations in North America and the Hopewell Hypothesis
- X-linked Nephrogenic Diabetes Insipidus: from the Ship Hopewell to RFLP Studies
- [Congenital Nephrogenic Diabetes Insipidus] (French)
- [Hereditary Nephrogenic Diabetes Insipidus] (French)
- [Molecular biological studies on patients with nephrogenic diabetes insipidus]. (Hungarian)
- [Nephrogenic Diabetes Insipidus] (Hungarian)
- [Pathological Aspects of Water Transport in the Collecting Ducts] (French)
- [Simultaneous Familial Occurrence of Distal Renal Tubular Acidosis, Polycystic Kidney and Nephrogenic Diabetes Insipidus] (Hungarian)
Used in 13 Article bodies
Used in 13 Article bodies
- A Novel Polymorphism in the Coding Region of the Vasopressin Type 2 Receptor Gene
- Analysis of Vasopressin Receptor Type II (V2R) Gene in Three Japanese Pedigrees with Congenital Nephrogenic Diabetes Insipidus: Identification of a Family with Complete Deletion of the V2R Gene
- Evidence that the Antidiuretic Substance in the Plasma of Children with Nephrogenic Diabetes Insipidus is Antidiuretic Hormone
- Hereditary Vasopressin Resistance in Man and Mouse
- Inborn Errors of Signal Transduction: Mutations in G Proteins and G Protein-coupled Receptors as a Cause of Disease
- Intracranial Calcification in Nephrogenic Diabetes Insipidus
- Molecular Analysis of X-Linked Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus Following High Dose Epirubicin Chemotherapy for Metastatic Soft Tissue Sarcoma [Letter]
- Nephrogenic Diabetes Insipidus in North America. The Hopewell Hypothesis
- Nephrogenic Diabetes Insipidus: A Cause of Severe Nonobstructive Urinary Tract Dilatation
- Nephrogenic Diabetes Insipidus: Transmitted by Females and Appearing During Infancy in Males
- Notes on Some Cases of Diabetes Insipidus with Marked Family and Hereditary Tendencies
- Proposed Cause of Marked Vasopressin Resistance in a Female with an X-Linked Recessive V2 Receptor Abnormality
Used in 58 Article translations
Used in 58 Article translations
- A Case of a Novel Mutant Vasopressin Receptor-Dependent Nephrogenic Diabetes Insipidus With Bilateral Non-Obstructive Hydronephrosis in a Middle Aged Man
- A Compartmental Model Predicts that Dietary Potassium Affects Lithium Dynamics in Rats
- A Congenital Defect of Water Metabolism
- Amphotericin B-Induced Partial Nephrogenic Diabetes Insipidus in a Child
- An Impaired Routing of Wild-type Aquaporin-2 after Tetramerization with an Aquaporin-2 Mutant Explains Dominant Nephrogenic Diabetes Insipidus
- Analysis of Vasopressin Receptor Type II (V2R) Gene in Three Japanese Pedigrees with Congenital Nephrogenic Diabetes Insipidus: Identification of a Family with Complete Deletion of the V2R Gene
- Aquaporins: From Physiology to Nephrogenic Diabetes Insipidus
- Autosomal Recessive Nephrogenic Diabetes Insipidus Caused by an Aquaporin-2 Mutation
- Biochemical Basis of Partial Nephrogenic Diabetes Insipidus Phenotypes
- Clinical Utility of Direct Mutation Testing for Congenital Nephrogenic Diabetes Insipidus in Families
- Cognitive and Psychosocial Functioning of Patients with Congenital Nephrogenic Diabetes Insipidus
- Congenital Nephrogenic Diabetes Insipidus
- Congenital Nephrogenic Diabetes Insipidus in an Adult
- Correlation between Magnetic Resonance Imaging of Posterior Pituitary and Neurohypophyseal Function in Children with Diabetes Insipidus
- Defects of G Protein-Coupled Signal Transduction in Human Disease
- Diabetes Insipidus [Bell]
- Differential Diagnosis and Pathophysiology of Diabetes Insipidus
- Discovery of Aquaporins: a Breakthrough in Research on Renal Water Transport
- Epinephrine and dDAVP Administration in Patients with Congenital Nephrogenic Diabetes Insipidus. Evidence for a pre-cyclic AMP V2 Receptor Defective Mechanism
- Evaluation and Management of Diabetes Insipidus
- Functional Characterization of Five V2 Vasopressin Receptor Gene Mutations
- G-Protein-Coupled Receptors: Molecular Mechanisms Involved in Receptor Activation and Selectivity of G-Protein Recognition
- Genetic Renal Diseases in Children
- Identification and Characterization of Aquaporin-2 Water Channel Mutations Causing Nephrogenic Diabetes Insipidus with Partial Vasopressin Response
- Impaired Aquaporin and Urea Transporter Expression in Rats with Adriamycin-Induced Nephrotic Syndrome
- Inborn Errors of Signal Transduction: Mutations in G Proteins and G Protein-coupled Receptors as a Cause of Disease
- Index of Suspicion. Case 2. Nephrogenic Diabetes Insipidus
- Indomethacin Treatment in Amphotericin B Induced Nephrogenic Diabetes Insipidus
- Intracanial Calcifications and Nephrogenic Diabetes Insipidus
- Linkage of X-linked Nephrogenic Diabetes Insipidus with DXS52, a Polymorphic DNA Marker
- Lithium-induced Down regulation of Aquaporin-2 Water Channel Expression in Rat Kidney Medulla
- Meniere's Disease in Congenital Nephrogenic Diabetes Insipidus: Report of Two Twins
- Molecular Analysis of X-Linked Nephrogenic Diabetes Insipidus
- Molecular Genetic Study of Congenital Nephrogenic Diabetes Insipidus and Rescue of Mutant Vasopressin V2 Receptor by Chemical Chaperones
- Molecular Insights into the Pathogenesis of Inherited Renal Tubular Disorders
- Nephrogenic Diabetes Insipidus (Bichet)
- Nephrogenic Diabetes Insipidus in Mice Lacking All Nitric Oxide Synthase Isoforms
- Nephrogenic Diabetes Insipidus--Prodromal Phase of Multiple Myeloma
- Nephrogenic Diabetes Insipidus: Clinical Symptoms, Pathogenesis, Genetics and Treatment
- Nephrogenic Diabetes Insipidus: Identification of the Genetic Defect
- Nephrogenic Diabetes Insipidus: Transmitted by Females and Appearing During Infancy in Males
- On Hereditary Diabetes Insipidus With Special Regard to a Sex-Linked Form
- Pathogenesis and Treatment of Autosomal-Dominant Nephrogenic Diabetes Insipidus Caused by an Aquaporin 2 Mutation
- Pathophysiology of Aquaporin-2 in Water Balance Disorders
- Pathophysiology of the Aquaporin Water Channels
- Pharmacological Chaperones Rescue Cell-Surface Expression and Function of Misfolded V2 Vasopressin Receptor Mutants
- Pharmacological Chaperones: Potential Treatment for Conformational Diseases
- Physiology and Pathophysiology of the Aquaporin-2 Water Channel
- Polyuria in Childhood
- Proposed Cause of Marked Vasopressin Resistance in a Female with an X-Linked Recessive V2 Receptor Abnormality
- Reconstitution of Mutant V2 Vasopressin Receptors by Adenovirus-mediated Gene Transfer
- Recurrent Dehydration in a Young Girl
- The Aquaporin Family of Water Channel Proteins in Clinical Medicine
- Three Novel AVPR2 Mutations in Three Japanese Families with X-Linked Nephrogenic Diabetes Insipidus
- Treatment of Nephrogenic Diabetes Insipidus with Hydrochlorothiazide and Amiloride
- Vasopressin Type-2 Receptor and Aquaporin-2 Water Channel Mutants in Nephrogenic Diabetes Insipidus
- Vasopressin V2 Receptor Mutants that Cause X-linked Nephrogenic Diabetes Insipidus: Analysis of Expression, Processing, and Function
- X-linked Nephrogenic Diabetes Insipidus: from the Ship Hopewell to RFLP Studies
Used in 9 Faq answers
Used in 9 Faq answers
- How can I contact other people who are dealing with NDI?
- Can NDI symptoms relapse for certain periods and then reappear?
- How can I help other families with NDI?
- How many people have NDI?
- I hear of persons being able to go without medication. I do not see that happening for my boys. Why is the disease different in each patient?
- Should females with NDI be medicated differently than males?
- What is the life expectancy of an NDI child?
- Will NDI ever go away?
- Will a male child with NDI pass it on to their children? Male or female?
Used in 38 Proceeding abstracts
Used in 38 Proceeding abstracts
- A defect in AQP2 phosphorylation at Ser256 in the Golgi apparatus might explain the molecular basis of the dominant form of NDI caused by the mutation E258K-AQP2
- A patient's perspective
- Action Mechanism of Pharmacological Chaperones Acting on the V2 Vasopressin Receptor in the Treatment of Nephrogenic Diabetes Insipidus
- An impaired routing of wild type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus
- Analysis of naturally occurring and in vitro mutations of the V2 receptor gene interfering with proper splicing
- Bartter syndrome with sensorineural deafness: molecular genetics
- Candesartan treatment prevents dysregulation of AQP2, BSC-1 and NaPi2 in ureteral obstruction-induced NDI
- Cell biological and functional analysis of five new Aquaporin-2 gene missense mutations in recessive Nephrogenic Diabetes Insipidus
- Clinical Data and Cell Biological Aspects of Mutations in Nephrogenic Diabetes Insipidus
- Clinical Phenotype and Molecular Characterization of A Mutant V2 Receptor Associated with Partial Congenital Nephrogenic Diabetes Insipidus
- Clinical analysis of eight Japanese patients with congenital nephrogenic diabetes insipidus
- Clinical and genetic approaches to the diagnosis of congenital polyuro-polydipsic syndromes
- Collecting Duct Specific Gene Regulation: Creation And Use of Transgenic Mouse Models
- Compartmentalization of NDI-causing vasopressin V2 receptor mutants in the early secretory pathway
- Complete deletions of the vasopressin type 2 receptor gene in nephrogenic diabetes insipidus
- Congenital (present a birth) severe diabetes insipidus. Most patients have nephrogenic diabetes insipidus (NDI), but some patients have autosomal recessive central (neurogenic) diabetes insipidus
- Consequences of tetramerization and expression levels of Aquaporin-2 in phenotype-genotype correlation studies in autosomal NDI
- Contribution of chloride channels in urine concentrating ability
- Decreased Aquaporin-2 Water Channel Expression in Acquired Nephrogenic Diabetes Insipidus
- Determination of the functionality of AQP2 missense mutants in recessive NDI
- Diversity of Nephrogenic Diabetes Insipidus Mutations and Importance of Early Recognition and Treatment
- Downregulation of renal aquaporins and sodium transporters in rats with bilateral ureteral obstruction (BUO) is prevented by a-MSH treatment
- Follow up of NDI patients and presentation of a case report
- Functional rescue of three vasopressin V2 receptor mutants causing nephrogenic diabetes insipidus by a second site suppressor mutation
- Functional studies of twelve mutant V2 vasopressin receptors related to nephrogenic diabetes insipidus: molecular basis of a mild clinical phenotype.
- Lack of AVP-induced phosphorylation of the Aquaporin-2 mutants AQP2-R254L and AQP2-R254Q explains dominant Nephrogenic Diabetes Insipidus
- Molecular mechanisms underlying dominant Nephrogenic Diabetes Insipidus caused by mutations in the AQP2 gene
- Mono-ubiquitination and missorting to lysosomes of the Aquaporin-2 water channel mutant AQP2-E258K explains dominant Nephrogenic Diabetes Insipidus
- Mutations in the vasopressin V2 receptor and aquaporin-2 genes in twelve families with congenital nephrogenic diabetes insipidus
- Naturally occurring and in vitro mutations defining the role of the NPXXY motif in the vasopressin V2 receptor
- Nephrogenic Diabetes Insipidus Mutation Database
- Pitfalls in the Differential Diagnosis of Nephrogenic Diabetes Insipidus.
- Routing and function of mutant AQP2 water channels in nephrogenic diabetes insipidus
- The Medical Geneticist's Perspective on NDI Research
- Thirteen Large Deletions/Rearrangements of the AVPR2 Gene Causing X-linked Nephrogenic Diabetes Insipidus
- Toward gene therapy for nephrogenic diabetes insipidus
- Transport Defects of V2 Receptor Mutants Found in Patients with X-linked Nephrogenic Diabetes Insipidus
- V2 vasopressin receptor function studied in mice and yeast
Used in 10 Proceeding translations
Used in 10 Proceeding translations
- An impaired routing of wild type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus
- Bartter syndrome with sensorineural deafness: molecular genetics
- Cell biological and functional analysis of five new Aquaporin-2 gene missense mutations in recessive Nephrogenic Diabetes Insipidus
- Chemical Chaperones as a Novel Therapeutic Strategy for NDI
- Consequences of tetramerization and expression levels of Aquaporin-2 in phenotype-genotype correlation studies in autosomal NDI
- Follow up of NDI patients and presentation of a case report
- High proportion of ROMK processing defects underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome
- Nephrogenic Diabetes Insipidus Mutation Database
- Progress in the function and structure of aquaporin-1 and aquaporin-2
- Rediscovery of Swedish Kindred with X-linked 'Vasopressin-Responsive' Diabetes Insipidus: Validation and Explanation of the Unusual Clinical Phenotype
Used in 232 Term definitions
Used in 232 Term definitions
- Microspora
- Muridae
- Mycobacterium avium-intracellulare
- Mycobacterium tuberculosis
- Niemann's disease
- Spanish influenza
- accident
- aging
- alcohol dependence
- amyloidosis
- ankylosis
- antiherpes
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- bone marrow transplant
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- bronchiolitis fibrosa obliterans
- camelpox
- cancer
- cardiomyopathy
- carrier
- case
- case study
- casuistics
- cell-mediated immunity
- chemotherapy
- chiropractic
- cholera
- chronic active hepatitis
- chronic agressive hepatitis
- cirrhosis of the liver
- coccidioidomycosis
- collagen diseases
- collagen disorder
- colloid
- compensate
- compensation
- complication
- contagion
- control
- control group
- control rats
- cosegregated
- cowpox
- crisis
- critical
- curative
- cure
- cystic fibrosis
- cytomegalic inclusion disease
- decline
- definition
- diagnose
- diagnosed
- diagnosing
- diagnosis
- diagnostic
- dicumarol
- differentiation
- diphtheria
- disposition
- distribution
- drug
- effluvium
- electrotherapy
- encephalopathy
- endemic
- endothelioid cells
- epidemic
- epididymo-orchitis
- equivalent
- eruption
- essential
- etiological
- etiologically
- etiologies
- etiology
- exacerbate
- examination
- exanthem
- familial Mediterranean fever
- fetor hepaticus
- fever
- generalized
- graft-versus-host reaction
- health
- healthy
- hepatic encephalopathy
- hepatitis B
- hepatitis C
- histiocytosis X
- histoplasmosis
- homeopathy
- hypersensitivity reaction
- hypersensitivity reactions
- immunocompromised
- immunopathology
- inborn error of metabolism
- inborn errors of metabolism
- incidence
- index case
- infect
- infected
- infection
- infectious disease
- infirmity
- influenza virus
- inoculate
- inoculation
- intervention
- invasion
- isolation
- kidney disorders
- late latent syphilis
- latent syphilis
- leprosy
- leukemia
- liver cancer
- liver cirrhosis
- liver transplant
- lymphadenopathy
- lysis
- lysosomal storage disease
- malaria
- medicine
- metastasis
- metastasize
- microbe
- mimetic
- mimic
- monkeypox
- mononeuropathy
- morbid
- morbid process
- multiple myeloma
- nephropathy
- nephrosis
- neurology
- non-Hodgkin's lymphoma
- obliterate
- obstructive nephropathy
- osteopathy
- pancreatitis
- pandemic
- pathogen
- pathogenesis
- pathogenic
- pathogenic organisms
- pathogenicity
- pathogens
- pathophysiology
- patient
- pest
- pharmacotherapeutics
- phase
- physical examination
- physical therapy
- polycystic disease of the kidneys
- practice
- predisposed
- predisposing
- predisposition
- preventive treatment
- primary hypothyroidism
- prodromal
- prodrome
- prognosis
- prophylactic
- prophylaxis
- protocol
- pulmonary tuberculosis
- quarantine
- radioiodine
- radiology
- radiotherapy
- rat
- reactive systemic amyloidosis
- regression
- relapse
- relapsed
- relapses
- relapsing
- remedy
- remission
- resistance
- resistant
- respiratory distress syndrome of the newborn
- respiratory syncytial viruses
- rheumatoid arthritis
- risk factors
- rubella
- sclerosis
- screen
- screened
- screening
- secondary or progressive coccidioidomycosis
- seizure
- seizures
- sensitivity
- sequela
- sickle cell anemia
- sickly
- sign
- simulate
- smallpox
- specific
- specificity
- spectrum
- stage
- state
- subclinical
- susceptibility
- sympathy
- symptom
- symptomatic
- symptoms
- systemic disease
- tarsal coalition
- therapeutics
- therapy
- thrombocytopenic purpura
- toxic microbe
- transmission
- transmitted
- transmitting
- treatment
- tuberculosis
- type
- type 1 diabetes mellitus
- variant
- victim
- virulence
- virus



