Hyperparathyroidism, the Glossary
Hyperparathyroidism is an increase in parathyroid hormone (PTH) levels in the blood.[1]
Table of Contents
123 relations: Alkaline phosphatase, Ascending limb of loop of Henle, Assessment of kidney function, Autonomy, Benign tumor, Bicarbonate, Bipolar disorder, Blood, Blood test, Bone density, Breast cancer, Calcifediol, Calcimimetic, Calciphylaxis, Calcitriol, Calcium, Calcium in biology, Calcium-sensing receptor, CDC73, Cholecalciferol, Chronic kidney disease, Cinacalcet, Cochrane (organisation), Collecting duct system, Constipation, CT scan, DDT, Depression (mood), Developed country, Diet (nutrition), Distal convoluted tubule, Dual-energy X-ray absorptiometry, Ectopia (medicine), Endocrine and Metabolic Diseases Information Service, Endocrine disease, Endocrinology, Endoderm, Familial hypocalciuric hypercalcemia, Fatigue, G protein-coupled receptor, Gastric bypass surgery, Genealogy, Granuloma, Human embryonic development, Hydroxyapatite, Hypercalcaemia, Hypercalciuria, Hyperchloremia, Hyperphosphatemia, Hyperthyroidism, ... Expand index (73 more) »
- Endocrine-related cutaneous conditions
- Parathyroid disorders
Alkaline phosphatase
The enzyme alkaline phosphatase (ALP, alkaline phenyl phosphatase) is a phosphatase with the physiological role of dephosphorylating compounds.
See Hyperparathyroidism and Alkaline phosphatase
Ascending limb of loop of Henle
Within the nephron of the kidney, the ascending limb of the loop of Henle is a segment of the heterogenous loop of Henle downstream of the descending limb, after the sharp bend of the loop.
See Hyperparathyroidism and Ascending limb of loop of Henle
Assessment of kidney function
Assessment of kidney function occurs in different ways, using the presence of symptoms and signs, as well as measurements using urine tests, blood tests, and medical imaging.
See Hyperparathyroidism and Assessment of kidney function
Autonomy
In developmental psychology and moral, political, and bioethical philosophy, autonomy is the capacity to make an informed, uncoerced decision.
See Hyperparathyroidism and Autonomy
Benign tumor
A benign tumor is a mass of cells (tumor) that does not invade neighboring tissue or metastasize (spread throughout the body).
See Hyperparathyroidism and Benign tumor
Bicarbonate
In inorganic chemistry, bicarbonate (IUPAC-recommended nomenclature: hydrogencarbonate) is an intermediate form in the deprotonation of carbonic acid.
See Hyperparathyroidism and Bicarbonate
Bipolar disorder
Bipolar disorder, previously known as manic depression, is a mental disorder characterized by periods of depression and periods of abnormally elevated mood that each last from days to weeks.
See Hyperparathyroidism and Bipolar disorder
Blood
Blood is a body fluid in the circulatory system of humans and other vertebrates that delivers necessary substances such as nutrients and oxygen to the cells, and transports metabolic waste products away from those same cells.
See Hyperparathyroidism and Blood
Blood test
A blood test is a laboratory analysis performed on a blood sample that is usually extracted from a vein in the arm using a hypodermic needle, or via fingerprick.
See Hyperparathyroidism and Blood test
Bone density
Bone density, or bone mineral density, is the amount of bone mineral in bone tissue.
See Hyperparathyroidism and Bone density
Breast cancer
Breast cancer is a cancer that develops from breast tissue.
See Hyperparathyroidism and Breast cancer
Calcifediol
Calcifediol, also known as calcidiol, 25-hydroxycholecalciferol, or 25-hydroxyvitamin D3 (abbreviated 25(OH)D3), is a form of vitamin D produced in the liver by hydroxylation of vitamin D3 (cholecalciferol) by the enzyme vitamin D 25-hydroxylase.
See Hyperparathyroidism and Calcifediol
Calcimimetic
A calcimimetic is a pharmaceutical drug that mimics the action of calcium on tissues, by allosteric activation of the calcium-sensing receptor that is expressed in various human organ tissues.
See Hyperparathyroidism and Calcimimetic
Calciphylaxis
Calciphylaxis, also known as calcific uremic arteriolopathy (CUA) or “Grey Scale”, is a rare syndrome characterized by painful skin lesions.
See Hyperparathyroidism and Calciphylaxis
Calcitriol
Calcitriol is the active form of vitamin D, normally made in the kidney.
See Hyperparathyroidism and Calcitriol
Calcium
Calcium is a chemical element; it has symbol Ca and atomic number 20.
See Hyperparathyroidism and Calcium
Calcium in biology
Calcium ions (Ca2+) contribute to the physiology and biochemistry of organisms' cells.
See Hyperparathyroidism and Calcium in biology
Calcium-sensing receptor
The calcium-sensing receptor (CaSR) is a Class C G-protein coupled receptor which senses extracellular levels of calcium ions.
See Hyperparathyroidism and Calcium-sensing receptor
CDC73
Cell division cycle 73, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae), also known as CDC73 and parafibromin, is a protein which in humans is encoded by the CDC73 gene.
See Hyperparathyroidism and CDC73
Cholecalciferol
Cholecalciferol, also known as vitamin D3 and colecalciferol, is a type of vitamin D that is made by the skin when exposed to UV-B light; it is found in some foods and can be taken as a dietary supplement.
See Hyperparathyroidism and Cholecalciferol
Chronic kidney disease
Chronic kidney disease (CKD) is a type of long-term kidney disease, in which either there is a gradual loss of kidney function occurs over a period of months to years, or abnormal kidney structure (with normal function).
See Hyperparathyroidism and Chronic kidney disease
Cinacalcet
Cinacalcet, sold under the brand name Sensipar among others, is a medication used to treat primary hyperparathyroidism, tertiary hyperparathyroidism and parathyroid carcinoma.
See Hyperparathyroidism and Cinacalcet
Cochrane (organisation)
Cochrane is a British international charitable organisation formed to synthesize medical research findings to facilitate evidence-based choices about health interventions involving health professionals, patients and policy makers.
See Hyperparathyroidism and Cochrane (organisation)
Collecting duct system
The collecting duct system of the kidney consists of a series of tubules and ducts that physically connect nephrons to a minor calyx or directly to the renal pelvis.
See Hyperparathyroidism and Collecting duct system
Constipation
Constipation is a bowel dysfunction that makes bowel movements infrequent or hard to pass.
See Hyperparathyroidism and Constipation
CT scan
A computed tomography scan (CT scan; formerly called computed axial tomography scan or CAT scan) is a medical imaging technique used to obtain detailed internal images of the body.
See Hyperparathyroidism and CT scan
DDT
Dichlorodiphenyltrichloroethane, commonly known as DDT, is a colorless, tasteless, and almost odorless crystalline chemical compound, an organochloride.
See Hyperparathyroidism and DDT
Depression (mood)
Depression is a mental state of low mood and aversion to activity.
See Hyperparathyroidism and Depression (mood)
Developed country
A developed country, or advanced country, is a sovereign state that has a high quality of life, developed economy, and advanced technological infrastructure relative to other less industrialized nations.
See Hyperparathyroidism and Developed country
Diet (nutrition)
In nutrition, diet is the sum of food consumed by a person or other organism.
See Hyperparathyroidism and Diet (nutrition)
Distal convoluted tubule
The distal convoluted tubule (DCT) is a portion of kidney nephron between the loop of Henle and the collecting tubule.
See Hyperparathyroidism and Distal convoluted tubule
Dual-energy X-ray absorptiometry
Dual-energy X-ray absorptiometry (DXA, or DEXA) is a means of measuring bone mineral density (BMD) using spectral imaging.
See Hyperparathyroidism and Dual-energy X-ray absorptiometry
Ectopia (medicine)
An ectopia is a displacement or malposition of an organ or other body part, which is then referred to as ectopic.
See Hyperparathyroidism and Ectopia (medicine)
The Endocrine and Metabolic Diseases Information Service is an information dissemination service of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).
See Hyperparathyroidism and Endocrine and Metabolic Diseases Information Service
Endocrine disease
Endocrine diseases are disorders of the endocrine system.
See Hyperparathyroidism and Endocrine disease
Endocrinology
Endocrinology (from endocrine + -ology) is a branch of biology and medicine dealing with the endocrine system, its diseases, and its specific secretions known as hormones.
See Hyperparathyroidism and Endocrinology
Endoderm
Endoderm is the innermost of the three primary germ layers in the very early embryo.
See Hyperparathyroidism and Endoderm
Familial hypocalciuric hypercalcemia
Familial hypocalciuric hypercalcemia (FHH) is an inherited condition that can cause hypercalcemia, a serum calcium level typically above 10.2 mg/dL; although uncommon.
See Hyperparathyroidism and Familial hypocalciuric hypercalcemia
Fatigue
Fatigue describes a state of tiredness (which is not sleepiness), exhaustion or loss of energy.
See Hyperparathyroidism and Fatigue
G protein-coupled receptor
G protein-coupled receptors (GPCRs), also known as seven-(pass)-transmembrane domain receptors, 7TM receptors, heptahelical receptors, serpentine receptors, and G protein-linked receptors (GPLR), form a large group of evolutionarily related proteins that are cell surface receptors that detect molecules outside the cell and activate cellular responses.
See Hyperparathyroidism and G protein-coupled receptor
Gastric bypass surgery
Gastric bypass surgery refers to a technique in which the stomach is divided into a small upper pouch and a much larger lower "remnant" pouch, where the small intestine is rearranged to connect to both.
See Hyperparathyroidism and Gastric bypass surgery
Genealogy
Genealogy is the study of families, family history, and the tracing of their lineages.
See Hyperparathyroidism and Genealogy
Granuloma
A granuloma is an aggregation of macrophages (along with other cells) that forms in response to chronic inflammation.
See Hyperparathyroidism and Granuloma
Human embryonic development
Human embryonic development or human embryogenesis is the development and formation of the human embryo.
See Hyperparathyroidism and Human embryonic development
Hydroxyapatite
Hydroxyapatite (IMA name: hydroxylapatite) (Hap, HAp, or HA) is a naturally occurring mineral form of calcium apatite with the formula, often written to denote that the crystal unit cell comprises two entities.
See Hyperparathyroidism and Hydroxyapatite
Hypercalcaemia
Hypercalcemia, also spelled hypercalcaemia, is a high calcium (Ca2+) level in the blood serum.
See Hyperparathyroidism and Hypercalcaemia
Hypercalciuria
Hypercalciuria is the condition of elevated calcium in the urine.
See Hyperparathyroidism and Hypercalciuria
Hyperchloremia
Hyperchloremia is an electrolyte disturbance in which there is an elevated level of chloride ions in the blood.
See Hyperparathyroidism and Hyperchloremia
Hyperphosphatemia
Hyperphosphatemia is an electrolyte disorder in which there is an elevated level of phosphate in the blood.
See Hyperparathyroidism and Hyperphosphatemia
Hyperthyroidism
Hyperthyroidism is the condition that occurs due to excessive production of thyroid hormones by the thyroid gland. Hyperparathyroidism and Hyperthyroidism are endocrine-related cutaneous conditions.
See Hyperparathyroidism and Hyperthyroidism
Hypocalcemia
Hypocalcemia is a medical condition characterized by low calcium levels in the blood serum.
See Hyperparathyroidism and Hypocalcemia
Hypoparathyroidism
Hypoparathyroidism is decreased function of the parathyroid glands with underproduction of parathyroid hormone (PTH). Hyperparathyroidism and Hypoparathyroidism are endocrine-related cutaneous conditions and parathyroid disorders.
See Hyperparathyroidism and Hypoparathyroidism
Immunoassay
An immunoassay (IA) is a biochemical test that measures the presence or concentration of a macromolecule or a small molecule in a solution through the use of an antibody (usually) or an antigen (sometimes).
See Hyperparathyroidism and Immunoassay
Kidney stone disease
Kidney stone disease, also known as renal calculus disease, nephrolithiasis or urolithiasis, is a crystallopathy where a solid piece of material (renal calculus) develops in the urinary tract.
See Hyperparathyroidism and Kidney stone disease
Lithium
Lithium is a chemical element; it has symbol Li and atomic number 3.
See Hyperparathyroidism and Lithium
Lithium (medication)
Certain lithium compounds, also known as lithium salts, are used as psychiatric medication, primarily for bipolar disorder and for major depressive disorder.
See Hyperparathyroidism and Lithium (medication)
Lymphoma
Lymphoma is a group of blood and lymph tumors that develop from lymphocytes (a type of white blood cell).
See Hyperparathyroidism and Lymphoma
Major depressive disorder
Major depressive disorder (MDD), also known as clinical depression, is a mental disorder characterized by at least two weeks of pervasive low mood, low self-esteem, and loss of interest or pleasure in normally enjoyable activities.
See Hyperparathyroidism and Major depressive disorder
Malabsorption
Malabsorption is a state arising from abnormality in absorption of food nutrients across the gastrointestinal (GI) tract.
See Hyperparathyroidism and Malabsorption
The mediastinum (from;: mediastina) is the central compartment of the thoracic cavity.
See Hyperparathyroidism and Mediastinum
MEN1
Menin is a protein that in humans is encoded by the MEN1 gene.
See Hyperparathyroidism and MEN1
Milk-alkali syndrome
Milk-alkali syndrome (MAS), also referred to as calcium-alkali syndrome, is the third most common cause of hypercalcemia.
See Hyperparathyroidism and Milk-alkali syndrome
Multiple endocrine neoplasia
Multiple endocrine neoplasia (abbreviated MEN) is a condition which encompasses several distinct syndromes featuring tumors of endocrine glands, each with its own characteristic pattern.
See Hyperparathyroidism and Multiple endocrine neoplasia
Multiple endocrine neoplasia type 1
Multiple endocrine neoplasia type 1 (MEN-1) is one of a group of disorders, the multiple endocrine neoplasias, that affect the endocrine system through development of neoplastic lesions in pituitary, parathyroid gland and pancreas. Hyperparathyroidism and multiple endocrine neoplasia type 1 are endocrine-related cutaneous conditions.
See Hyperparathyroidism and Multiple endocrine neoplasia type 1
Multiple endocrine neoplasia type 2
Multiple endocrine neoplasia type 2 (also known as "Pheochromocytoma (codons 630 and 634) and amyloid producing medullary thyroid carcinoma", "PTC syndrome," and "Sipple syndrome") is a group of medical disorders associated with tumors of the endocrine system. Hyperparathyroidism and Multiple endocrine neoplasia type 2 are endocrine-related cutaneous conditions.
See Hyperparathyroidism and Multiple endocrine neoplasia type 2
Multiple myeloma
Multiple myeloma (MM), also known as plasma cell myeloma and simply myeloma, is a cancer of plasma cells, a type of white blood cell that normally produces antibodies.
See Hyperparathyroidism and Multiple myeloma
Myalgia
Myalgia or muscle pain is a painful sensation evolving from muscle tissue.
See Hyperparathyroidism and Myalgia
Nausea
Nausea is a diffuse sensation of unease and discomfort, sometimes perceived as an urge to vomit.
See Hyperparathyroidism and Nausea
Neolithic
The Neolithic or New Stone Age (from Greek νέος 'new' and λίθος 'stone') is an archaeological period, the final division of the Stone Age in Europe, Asia and Africa.
See Hyperparathyroidism and Neolithic
Nephrocalcinosis
Nephrocalcinosis, once known as Albright's calcinosis after Fuller Albright, is a term originally used to describe the deposition of poorly soluble calcium salts in the renal parenchyma due to hyperparathyroidism.
See Hyperparathyroidism and Nephrocalcinosis
Nephron
The nephron is the minute or microscopic structural and functional unit of the kidney.
See Hyperparathyroidism and Nephron
Nuclear medicine
Nuclear medicine, or nucleology, is a medical specialty involving the application of radioactive substances in the diagnosis and treatment of disease.
See Hyperparathyroidism and Nuclear medicine
Osteoblast
Osteoblasts (from the Greek combining forms for "bone", ὀστέο-, osteo- and βλαστάνω, blastanō "germinate") are cells with a single nucleus that synthesize bone.
See Hyperparathyroidism and Osteoblast
Osteoclast
An osteoclast is a type of bone cell that breaks down bone tissue.
See Hyperparathyroidism and Osteoclast
Osteocyte
An osteocyte, an oblate shaped type of bone cell with dendritic processes, is the most commonly found cell in mature bone.
See Hyperparathyroidism and Osteocyte
Osteomalacia
Osteomalacia is a disease characterized by the softening of the bones caused by impaired bone metabolism primarily due to inadequate levels of available phosphate, calcium, and vitamin D, or because of resorption of calcium.
See Hyperparathyroidism and Osteomalacia
Osteopenia
Osteopenia, known as "low bone mass" or "low bone density", is a condition in which bone mineral density is low.
See Hyperparathyroidism and Osteopenia
Osteoporosis
Osteoporosis is a systemic skeletal disorder characterized by low bone mass, micro-architectural deterioration of bone tissue leading to more porous bone, and consequent increase in fracture risk.
See Hyperparathyroidism and Osteoporosis
Osteoprotegerin
Osteoprotegerin (OPG), also known as osteoclastogenesis inhibitory factor (OCIF) or tumour necrosis factor receptor superfamily member 11B (TNFRSF11B), is a cytokine receptor of the tumour necrosis factor (TNF) receptor superfamily encoded by the TNFRSF11B gene.
See Hyperparathyroidism and Osteoprotegerin
Pancreatic disease
Pancreatic diseases are diseases that affect the pancreas, an organ in most vertebrates and in humans and other mammals located in the abdomen.
See Hyperparathyroidism and Pancreatic disease
Pancreatitis
Pancreatitis is a condition characterized by inflammation of the pancreas.
See Hyperparathyroidism and Pancreatitis
Paracellular transport
Paracellular transport refers to the transfer of substances across an epithelium by passing through the intercellular space between the cells.
See Hyperparathyroidism and Paracellular transport
Parafollicular cell
Parafollicular cells, also called C cells, are neuroendocrine cells in the thyroid.
See Hyperparathyroidism and Parafollicular cell
Parathyroid adenoma
A parathyroid adenoma is a benign tumor of the parathyroid gland.
See Hyperparathyroidism and Parathyroid adenoma
Parathyroid carcinoma
Parathyroid carcinoma is a rare cancer resulting in parathyroid adenoma to carcinoma progression.
See Hyperparathyroidism and Parathyroid carcinoma
Parathyroid gland
Parathyroid glands are small endocrine glands in the neck of humans and other tetrapods.
See Hyperparathyroidism and Parathyroid gland
Parathyroid hormone
Parathyroid hormone (PTH), also called parathormone or parathyrin, is a peptide hormone secreted by the parathyroid glands that regulates the serum calcium concentration through its effects on bone, kidney, and intestine.
See Hyperparathyroidism and Parathyroid hormone
Parathyroidectomy
Parathyroidectomy is the surgical removal of one or more of the (usually) four parathyroid glands.
See Hyperparathyroidism and Parathyroidectomy
Pathologic fracture
A pathologic fracture is a bone fracture caused by weakness of the bone structure that leads to decrease mechanical resistance to normal mechanical loads.
See Hyperparathyroidism and Pathologic fracture
Peptic ulcer disease
Peptic ulcer disease is a break in the inner lining of the stomach, the first part of the small intestine, or sometimes the lower esophagus.
See Hyperparathyroidism and Peptic ulcer disease
PET-CT
Positron emission tomography–computed tomography (better known as PET-CT or PET/CT) is a nuclear medicine technique which combines, in a single gantry, a positron emission tomography (PET) scanner and an x-ray computed tomography (CT) scanner, to acquire sequential images from both devices in the same session, which are combined into a single superposed (co-registered) image.
See Hyperparathyroidism and PET-CT
Pharyngeal pouch (embryology)
In the embryonic development of vertebrates, pharyngeal pouches form on the endodermal side between the pharyngeal arches.
See Hyperparathyroidism and Pharyngeal pouch (embryology)
Pheochromocytoma
Pheochromocytoma is a rare tumor of the adrenal medulla composed of chromaffin cells and is part of the paraganglioma (PGL) family of tumors, being defined as an intra-adrenal PGL.
See Hyperparathyroidism and Pheochromocytoma
Phosphate
In chemistry, a phosphate is an anion, salt, functional group or ester derived from a phosphoric acid.
See Hyperparathyroidism and Phosphate
Phosphate binder
Phosphate binders are medications used to reduce the absorption of dietary phosphate; they are taken along with meals and snacks.
See Hyperparathyroidism and Phosphate binder
Polydipsia
Polydipsia is excessive thirst or excess drinking.
See Hyperparathyroidism and Polydipsia
Polyuria
Polyuria is excessive or an abnormally large production or passage of urine (greater than 2.5 L or 3 L over 24 hours in adults).
See Hyperparathyroidism and Polyuria
Primary hyperparathyroidism
Primary hyperparathyroidism (or PHPT) is a medical condition where the parathyroid gland (or a benign tumor within it) produce excess amounts of parathyroid hormone (PTH). Hyperparathyroidism and Primary hyperparathyroidism are parathyroid disorders.
See Hyperparathyroidism and Primary hyperparathyroidism
Proximal tubule
The proximal tubule is the segment of the nephron in kidneys which begins from the renal pole of the Bowman's capsule to the beginning of loop of Henle.
See Hyperparathyroidism and Proximal tubule
Racquet nail
In racquet nails (also known as brachyonychia, nail en raquette, and racquet thumb), the nail plate is flattened, the end of the thumb is widened and flattened, and the distal phalanx is abnormally short.
See Hyperparathyroidism and Racquet nail
RANKL
Receptor activator of nuclear factor kappa- ligand (RANKL), also known as tumor necrosis factor ligand superfamily member 11 (TNFSF11), TNF-related activation-induced cytokine (TRANCE), osteoprotegerin ligand (OPGL), and osteoclast differentiation factor (ODF), is a protein that in humans is encoded by the TNFSF11 gene.
See Hyperparathyroidism and RANKL
Renal osteodystrophy
Renal osteodystrophy is currently defined as an alteration of bone morphology in patients with chronic kidney disease (CKD).
See Hyperparathyroidism and Renal osteodystrophy
Renal ultrasonography
Renal ultrasonography (Renal US) is the examination of one or both kidneys using medical ultrasound.
See Hyperparathyroidism and Renal ultrasonography
RET proto-oncogene
The RET proto-oncogene encodes a receptor tyrosine kinase for members of the glial cell line-derived neurotrophic factor (GDNF) family of extracellular signalling molecules.
See Hyperparathyroidism and RET proto-oncogene
Rickets
Rickets, scientific nomenclature: rachitis (from Greek, meaning 'in or of the spine'), is a condition that results in weak or soft bones in children and is caused by either dietary deficiency or genetic causes.
See Hyperparathyroidism and Rickets
Saline (medicine)
Saline (also known as saline solution) is a mixture of sodium chloride (salt) and water.
See Hyperparathyroidism and Saline (medicine)
Secondary hyperparathyroidism
Secondary hyperparathyroidism is the medical condition of excessive secretion of parathyroid hormone (PTH) by the parathyroid glands in response to hypocalcemia (low blood calcium levels), with resultant hyperplasia of these glands. Hyperparathyroidism and Secondary hyperparathyroidism are parathyroid disorders.
See Hyperparathyroidism and Secondary hyperparathyroidism
Sestamibi parathyroid scan
A sestamibi parathyroid scan is a procedure in nuclear medicine which is performed to localize parathyroid adenoma, which causes Hyperparathyroidism.
See Hyperparathyroidism and Sestamibi parathyroid scan
Signs and symptoms
Signs and symptoms are the observed or detectable signs, and experienced symptoms of an illness, injury, or condition.
See Hyperparathyroidism and Signs and symptoms
Surgery
Surgery is a medical specialty that uses manual and instrumental techniques to diagnose or treat pathological conditions (e.g., trauma, disease, injury, malignancy), to alter bodily functions (i.e., malabsorption created by bariatric surgery such as gastric bypass), to reconstruct or improve aesthetics and appearance (cosmetic surgery), or to remove unwanted tissues (body fat, glands, scars or skin tags) or foreign bodies.
See Hyperparathyroidism and Surgery
Systematic review
A systematic review is a scholarly synthesis of the evidence on a clearly presented topic using critical methods to identify, define and assess research on the topic.
See Hyperparathyroidism and Systematic review
Tertiary hyperparathyroidism
Tertiary hyperparathyroidism is a condition involving the overproduction of the hormone, parathyroid hormone, produced by the parathyroid glands. Hyperparathyroidism and Tertiary hyperparathyroidism are parathyroid disorders.
See Hyperparathyroidism and Tertiary hyperparathyroidism
Thiazide
Thiazide refers to both a class of sulfur-containing organic molecules and a class of diuretics based on the chemical structure of benzothiadiazine.
See Hyperparathyroidism and Thiazide
Thyroid
The thyroid, or thyroid gland, is an endocrine gland in vertebrates.
See Hyperparathyroidism and Thyroid
Transcellular transport
Transcellular transport involves the transportation of solutes by a cell through a cell.
See Hyperparathyroidism and Transcellular transport
Ultimopharyngeal body
The ultimopharyngeal body, or ultimobranchial body or ultimobranchial gland is a small organ found in the neck region of many animals.
See Hyperparathyroidism and Ultimopharyngeal body
Urinary calcium
Urinary calcium is calcium in the urine.
See Hyperparathyroidism and Urinary calcium
Vitamin D
Vitamin D is a group of fat-soluble secosteroids responsible for increasing intestinal absorption of calcium, magnesium, and phosphate, and for many other biological effects.
See Hyperparathyroidism and Vitamin D
Vitamin D deficiency
Vitamin D deficiency or hypovitaminosis D is a vitamin D level that is below normal. It most commonly occurs in people when they have inadequate exposure to sunlight, particularly sunlight with adequate ultraviolet B rays (UVB). Vitamin D deficiency can also be caused by inadequate nutritional intake of vitamin D; disorders that limit vitamin D absorption; and disorders that impair the conversion of vitamin D to active metabolites, including certain liver, kidney, and hereditary disorders.
See Hyperparathyroidism and Vitamin D deficiency
Vitamin D receptor
The vitamin D receptor (VDR also known as the calcitriol receptor) is a member of the nuclear receptor family of transcription factors.
See Hyperparathyroidism and Vitamin D receptor
Vomiting
Vomiting (also known as emesis and throwing up) is the involuntary, forceful expulsion of the contents of one's stomach through the mouth and sometimes the nose.
See Hyperparathyroidism and Vomiting
Weakness
Weakness is a symptom of many different medical conditions.
See Hyperparathyroidism and Weakness
25-Hydroxyvitamin D 1-alpha-hydroxylase
25-Hydroxyvitamin D 1-alpha-hydroxylase (VD 1A hydroxylase) also known as calcidiol 1-monooxygenase or cytochrome p450 27B1 (CYP27B1) or simply 1-alpha-hydroxylase is a cytochrome P450 enzyme that in humans is encoded by the CYP27B1 gene.
See Hyperparathyroidism and 25-Hydroxyvitamin D 1-alpha-hydroxylase
See also
- ANOTHER syndrome
- Acanthosis nigricans
- Acromegaly
- Addison's disease
- Adrenocortical carcinoma
- Congenital adrenal hyperplasia
- Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency
- Congenital iodine deficiency syndrome
- Endocrine system
- Excess ovarian androgen release syndrome
- Glucocorticoid deficiency
- Glucocorticoid deficiency 1
- Growth hormone deficiency
- Hyperparathyroidism
- Hyperprolactinemic SAHA syndrome
- Hyperthyroidism
- Hypoparathyroidism
- Hypopituitarism
- Infertility in polycystic ovary syndrome
- Isolated growth hormone deficiency
- Late onset congenital adrenal hyperplasia
- Leydig cell tumour
- Multiple endocrine neoplasia type 1
- Multiple endocrine neoplasia type 2
- Multiple endocrine neoplasia type 2B
- Myxedema
- Persistent adrenarche syndrome
- Polycystic ovary syndrome
- SAHA syndrome
- Sertoli cell tumour
- Sertoli–Leydig cell tumour
Parathyroid disorders
- Hyperparathyroidism
- Hypoparathyroidism
- Osteitis fibrosa cystica
- Parathyroid disease
- Parathyroiditis
- Primary hyperparathyroidism
- Secondary hyperparathyroidism
- Tertiary hyperparathyroidism
References
[1] https://en.wikipedia.org/wiki/Hyperparathyroidism
Also known as Hyper-PTH, HyperPTH, Hyperparathyroidism,, Sestamibi scan for diagnosing hyperparathyroidism.
, Hypocalcemia, Hypoparathyroidism, Immunoassay, Kidney stone disease, Lithium, Lithium (medication), Lymphoma, Major depressive disorder, Malabsorption, Mediastinum, MEN1, Milk-alkali syndrome, Multiple endocrine neoplasia, Multiple endocrine neoplasia type 1, Multiple endocrine neoplasia type 2, Multiple myeloma, Myalgia, Nausea, Neolithic, Nephrocalcinosis, Nephron, Nuclear medicine, Osteoblast, Osteoclast, Osteocyte, Osteomalacia, Osteopenia, Osteoporosis, Osteoprotegerin, Pancreatic disease, Pancreatitis, Paracellular transport, Parafollicular cell, Parathyroid adenoma, Parathyroid carcinoma, Parathyroid gland, Parathyroid hormone, Parathyroidectomy, Pathologic fracture, Peptic ulcer disease, PET-CT, Pharyngeal pouch (embryology), Pheochromocytoma, Phosphate, Phosphate binder, Polydipsia, Polyuria, Primary hyperparathyroidism, Proximal tubule, Racquet nail, RANKL, Renal osteodystrophy, Renal ultrasonography, RET proto-oncogene, Rickets, Saline (medicine), Secondary hyperparathyroidism, Sestamibi parathyroid scan, Signs and symptoms, Surgery, Systematic review, Tertiary hyperparathyroidism, Thiazide, Thyroid, Transcellular transport, Ultimopharyngeal body, Urinary calcium, Vitamin D, Vitamin D deficiency, Vitamin D receptor, Vomiting, Weakness, 25-Hydroxyvitamin D 1-alpha-hydroxylase.