97 diseases · 13 high-burden in India
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders…
Congenital hypothyroidism (CH) is a thyroid hormone deficiency present at birth. If…
A diabetic foot disease is any condition that results directly from peripheral artery…
Dyslipidemia is a metabolic disorder characterized by abnormally high or low amounts of…
A goitre is a swelling in the neck resulting from an enlarged thyroid gland. A goitre can…
Hirsutism is excessive body hair on parts of the body where hair is normally absent or…
Hypothyroidism is an endocrine disease in which the thyroid gland does not produce enough…
Insulin resistance (IR) is a pathological response in which cells in insulin-sensitive…
Iodine deficiency is a lack of the trace element iodine, an essential nutrient in the…
Metabolic syndrome is a clustering of at least three of the following five medical…
Obesity is a medical condition, considered a disease by multiple organizations, in which…
Sheehan's syndrome, also known as postpartum pituitary gland necrosis, occurs when the…
Thyroid nodules are nodules which commonly arise within an otherwise normal thyroid…
Acromegaly is a disorder that results in excess growth of certain parts of the human…
Addison's disease, also known as primary adrenal insufficiency, is a rare long-term…
Adrenal crisis, also known as Addisonian crisis or acute adrenal insufficiency, is a…
Adrenocortical carcinoma (ACC) is an aggressive cancer originating in the cortex of the…
Alkaptonuria is a rare inherited genetic disease which is caused by a mutation in the HGD…
Alpha-mannosidosis is a lysosomal storage disorder, first described by Swedish physician…
Aspartylglucosaminuria (AGU) is an inherited disease that is characterized by a decline…
Beckwith–Wiedemann syndrome is an overgrowth disorder usually present at birth,…
Biotinidase deficiency is an autosomal recessive metabolic disorder in which biotin is…
Carcinoid syndrome is a paraneoplastic syndrome comprising the signs and symptoms that…
Carney complex and its subsets LAMB syndrome and NAME syndrome are autosomal dominant…
Carnitine palmitoyltransferase II deficiency, sometimes shortened to CPT-II or CPT2, is…
Primary aldosteronism (PA), also known as primary hyperaldosteronism, is the excess…
Cushing's syndrome is a collection of signs and symptoms due to prolonged exposure to…
Diabetes insipidus (DI) is a condition characterized by large amounts of dilute urine and…
Euthyroid sick syndrome (ESS) is a state of adaptation or dysregulation of thyrotropic…
Familial hypercholesterolemia (FH) is a genetic disorder characterized by high…
Familial hypocalciuric hypercalcemia (FHH) is an inherited condition that can cause…
Farber disease is an extremely rare, progressive, autosomal recessive lysosomal storage…
Fucosidosis is a rare lysosomal storage disorder in which the FUCA1 gene experiences…
Galactosemia is a rare genetic metabolic disorder that affects an individual's ability to…
Gigantism, also known as giantism, is a condition characterized by excessive growth and…
Glutaric acidemia type 1 (GA1) is an inherited disorder in which the body is unable to…
Graves' disease, also known as toxic diffuse goiter or Basedow's disease, is an…
Graves' ophthalmopathy, also known as thyroid eye disease (TED), is an autoimmune…
Hashimoto's thyroiditis, also known as chronic lymphocytic thyroiditis, Hashimoto's…
Hereditary fructose intolerance (HFI) is an inborn error of fructose metabolism caused by…
Homocystinuria (HCU) is an inherited disorder of the metabolism of the amino acid…
Hunter syndrome, or mucopolysaccharidosis type II, is a rare inherited lysosomal storage…
Hypercalcaemia, also spelt hypercalcemia (US), is a high calcium (Ca2+) level in the…
Hyperkalemia is an elevated level of potassium (K+) in the blood. Normal potassium levels…
Hypermagnesemia is an electrolyte disorder in which there is a high level of magnesium in…
Hyperparathyroidism is an increase in parathyroid hormone (PTH) levels in the blood. This…
Hyperphosphatemia is an electrolyte disorder in which there is an elevated level of…
Hyperprolactinaemia is a condition characterized by abnormally high levels of prolactin…
Hyperthyroidism is a endocrine disease in which the thyroid gland produces excessive…
Hypoaldosteronism is an endocrinological disorder characterized by decreased levels of…
Hypocalcemia (US) or hypocalcaemia (UK) is a medical condition characterized by low…
Hypoglycemia, also spelled hypoglycaemia or hypoglycæmia, sometimes called low blood…
Hypokalemia is a low level of potassium (K+) in the blood serum. Mild low potassium does…
Hyponatremia or hyponatraemia is a low concentration of sodium in the blood. It is…
Hypoparathyroidism is decreased function of the parathyroid glands with underproduction…
Hypophosphatemia is an electrolyte disorder in which there is a low level of phosphate in…
Hypopituitarism is the decreased (hypo) secretion of one or more of the eight hormones…
An insulinoma is a tumour of the pancreas that is derived from beta cells and secretes…
Isovaleric acidemia is a rare autosomal recessive metabolic disorder which disrupts or…
Kallmann syndrome (KS) is a genetic disorder that prevents a person from starting or…
Laron syndrome (LS), also known as growth hormone insensitivity or growth hormone…
Maple syrup urine disease (MSUD) is a rare, inherited metabolic disorder that affects the…
Maroteaux–Lamy syndrome, or mucopolysaccharidosis type VI (MPS-VI), is an inherited…
McCune–Albright syndrome is a complex genetic disorder affecting the bone, skin and…
Medullary thyroid cancer is a form of thyroid carcinoma which originates from the…
Methylmalonic acidemias, also called methylmalonic acidurias, are a group of inherited…
Morquio syndrome, also known as mucopolysaccharidosis type IV, is a rare metabolic…
Multiple endocrine neoplasia is a condition which encompasses several distinct syndromes…
Multiple endocrine neoplasia type 1 is one of a group of disorders, the multiple…
Multiple endocrine neoplasia type 2 is a group of medical disorders associated with…
Nesidioblastosis is a controversial medical term for hyperinsulinemic hypoglycemia…
Ornithine transcarbamylase deficiency also known as OTC deficiency is the most common…
Pendred syndrome is a genetic disorder leading to congenital bilateral sensorineural…
Pheochromocytoma is a rare tumor of the adrenal medulla composed of chromaffin cells and…
POEMS syndrome is a rare paraneoplastic syndrome caused by a clone of aberrant plasma…
In medicine, precocious puberty is puberty occurring at an unusually early age. In most…
A prolactinoma is a tumor (adenoma) of the pituitary gland that produces the hormone…
Propionic acidemia, also known as propionic aciduria or propionyl-CoA carboxylase…
Pseudohypoaldosteronism (PHA) is a condition that mimics hypoaldosteronism. Two major…
Pseudohypoparathyroidism is a rare autosomal dominant genetic condition associated…
Riedel's thyroiditis, is a chronic form of thyroiditis. It is now believed that Riedel's…
Sanfilippo syndrome, also known as mucopolysaccharidosis type III, is a rare lifelong…
Schindler disease, also known as Kanzaki disease and alpha-N-acetylgalactosaminidase…
Syndrome of inappropriate antidiuretic hormone secretion (SIADH), also known as the…
Mucolipidosis type I is an inherited lysosomal storage disease that results from a…
Silver–Russell syndrome (SRS), also called Silver–Russell dwarfism, is a rare congenital…
Smith–Lemli–Opitz syndrome is an inborn error of cholesterol synthesis. It is an…
Subacute thyroiditis refers to a temporal classification of the different forms of…
A thyroglossal cyst or thyroglossal duct cyst is a fibrous cyst that forms from a…
Thyroid cancer is cancer that develops from the tissues of the thyroid gland. It is a…
Thyroid storm is a rare but severe and life-threatening complication of hyperthyroidism.…
Thyrotoxic periodic paralysis (TPP) is a rare condition featuring attacks of muscle…
Tyrosinemia or tyrosinaemia is an error of metabolism, usually inborn, in which the body…
Waterhouse–Friderichsen syndrome (WFS) is defined as adrenal gland failure due to…
Wolfram syndrome, also called DIDMOAD, is a rare autosomal-recessive genetic disorder…
Lysosomal acid lipase deficiency or Wolman disease, is an autosomal recessive inborn…
Zellweger syndrome is a rare congenital disorder characterized by the reduction or…