Search Result

Top
1601 to 1640 of 3021 Prev 1 ... 36 37 38 39 40 41 42 43 44 45 46 ... 76 Next
Entry Name Description Category Pathway
H01605 Myelofibrosis Myelofibrosis (MF), one of the three classic Philadelphia-chromosome-negative myeloproliferative neoplasms (MPNs), is characterized by symptoms mainly derived from anemia and splenomegaly and constitutional ... Cancer
H01606 Polymyalgia rheumatica Polymyalgia rheumatica (PMR) is a relatively common inflammatory rheumatic disease in people older than 50 years of age. PMR is a clinical condition defined as the presence of inflammatory pain in the ... Musculoskeletal disease
H01607 Galactorrhea Galactorrhea is a discharge of milk or a milk-like secretion from the breast in the absence of parturition or beyond six months' post-partum in a nonbreastfeeding woman. The condition is more common in ... Reproductive system disease
H01608 Cervical dystonia
Spasmodic torticollis
Cervical dystonia (CD), formerly referred to as spasmodic torticollis, is a condition characterized by simultaneous and sustained contractions of both agonist and antagonist muscles of the neck, which ... Nervous system disease
H01609 Insomnia Insomnia is a common disorder with a prevalence of about 10% in the general population. The most common complaints related to insomnia are difficulty initiating sleep (sleep-onset insomnia), difficulty ... Nervous system disease
H01610 Clonorchiasis Clonorchiasis is an infectious disease of the biliary passages caused by Clonorchis sinensis of the family Opisthorchiidae. Clonorchis sinensis, the most common human liver fluke, is endemic in East Asia ... Parasitic infectious disease
H01611 Alcohol dependence Alcohol dependence (AD) is a chronic but often disease that includes problems in controlling one's drinking, being preoccupied with alcohol, continuing to use alcohol even when it causes problems, having ... Mental and behavioural disorder hsa05034 Alcoholism
H01612 Essential thrombocythemia
Essential thrombocytosis
Thrombocythemia
Essential thrombocythemia (ET) is one of the myeloproliferative neoplasms (MPNs), a group of clonal stem cell disorders with similarities at the phenotypic and molecular level. ET is characterized by an ... Hematologic disease
H01613 Follicular lymphoma Follicular lymphoma (FL) is generally an indolent B cell lymphoproliferative disorder of transformed follicular center B cells. FL is characterized by diffuse lymphoadenopathy, bone marrow involvement ... Cancer
H01614 Multiple system atrophy Multiple system atrophy (MSA) is an intractable neurodegenerative disease characterized by autonomic failure in addition to various combinations of parkinsonism, cerebellar ataxia, and pyramidal dysfunction ... Neurodegenerative disease
H01615 Irritable bowel syndrome Irritable bowel syndrome (IBS) is a common functional gastrointestinal disorder. It is characterized by symptoms of abdominal pain, bloating, and abnormal bowel movements, such as diarrhea or constipation ... Digestive system disease
H01616 Spinocerebellar degeneration Spinocerebellar degenerations are neurodegenerative diseases that involve the cerebellum, brain stem, spinal cord, and basal ganglia to various degrees. Patients display limb and truncal ataxia, dysarthria ... Neurodegenerative disease
H01617 Foodborne trematodiasis
Foodborne trematode infection
Foodborne trematode infections, which are caused by four main genera: Clonorchis spp. that cause clonorchiasis, Opisthorchis spp. that cause opisthorchiasis, Fasciola spp. that cause fascioliasis and Paragonimus ... Parasitic infectious disease
H01618 Pituitary gigantism Pituitary gigantism is very rare conditions resulting from excessive secretion of growth hormone (GH). Most cases are due to benign pituitary adenomas. Nonadenomatous GH excess is exceptional but occasionally ... Endocrine and metabolic disease
H01619 Primary pulmonary hypertension Primary pulmonary hypertension (PPH) is a progressive disorder characterised by raised pulmonary-artery pressures with pathological changes in precapillary pulmonary arteries. Cardiovascular disease
H01620 Raynaud syndrome Raynaud syndrome (RS) is characterized by episodic digital ischemia induced by cold or emotional stress. Pathophysiologic mechanisms include temporary vasospasm and fixed digital artery obstruction. Although ... Cardiovascular disease
H01621 Pulmonary arterial hypertension Pulmonary arterial hypertension (PAH) is a progressive disorder in which endothelial dysfunction and vascular remodeling obstruct small pulmonary arteries, resulting in increased pulmonary vascular resistance ... Cardiovascular disease
H01622 Chronic thromboembolic pulmonary hypertension Chronic thromboembolic pulmonary hypertension (CTEPH) is classified as group 4 pulmonary hypertension (PH) by the World Health Organization. It is a rare, but underdiagnosed, complication of acute pulmonary ... Cardiovascular disease
H01623 MDPL syndrome
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy (MDPL) syndrome is a rare autosomal dominant systemic disorder recently described. It has been reported that mutations in POLD1 cause ... Congenital malformation
H01624 Postherpetic neuralgia Herpes zoster (HZ) presents as a rash of 2-3 weeks duration in immunocompetent patients that is accompanied by moderate or severe pain. In some patients, pain does not resolve when the rash heals but continues ... Viral infectious disease
H01625 Buerger disease
Thromboangiitis obliterans
Buerger disease, also known as thromboangiitis obliterans, is a nonatherosclerotic, inflammatory disease that most commonly affects the small and medium-sized arteries and veins in the upper and lower ... Immune system disease
H01626 Arteriosclerosis obliterans Arteriosclerosis obliterans (ASO) is one of the most common peripheral vascular diseases that causes ischemic symptoms of the lower limbs. Symptoms include discomfort, numbness, intermittent claudication ... Cardiovascular disease
H01628 Opisthorchiasis Opisthorchiasis comprises diverse clinical symptoms caused by infections with Opisthorchis felineus or Opisthorchis viverrini liver flukes, which are transmitted by eating infected raw or undercooked fish ... Parasitic infectious disease
H01629 Chronic arterial occlusive disease Chronic arterial occlusive disease is a highly prevalent peripheral vascular disorder. This disease is caused by arteriosclerosis obliterans (ASO), thromboangiitis obliterans (Buerger's disease), primary ... Cardiovascular disease
H01630 Patent ductus arteriosus Patent ductus arteriosus (PDA) is a common congenital heart defect with both inherited and acquired causes. The ductus arteriosus (DA) is a fetal specific vascular connection between the main pulmonary ... Congenital malformation
H01631 Acute heart failure Acute heart failure (AHF) can be defined as a heterogeneous syndrome of signs and symptoms of new-onset or gradual/rapidly worsening heart failure (HF), requiring urgent therapy. Intrinsic cardiac abnormalities ... Cardiovascular disease
H01632 Angina pectoris Angina pectoris is defined as cardiac-induced pain arising from a lack of myocardial oxygen. "Angina" is used to describe clinical symptoms such as discomfort in the chest, jaw, shoulder, back, or arms ... Cardiovascular disease
H01633 High blood pressure
Hypertension
High blood pressure (hypertension) is the most frequent classic cardiovascular risk factor and accounts for a large proportion of cardiovascular mortality, the main cause of death worldwide. Hypertension ... Cardiovascular disease
H01634 Peptic ulcer Peptic ulcer is a common disorder of gastrointestinal system characterized by mucosal damage secondary to pepsin and gastric acid secretion. It usually occurs in the stomach and proximal duodenum. Typical ... Digestive system disease
H01635 Hyperlipidemia Dyslipidemia is a condition characterized by either an increase or decrease in concentration of lipids in the blood. Hyperlipidemia, which refers to an increase in cholesterol, triglyceride (TG), or both ... Endocrine and metabolic disease
H01636 Fibromyalgia
Fibromyalgia syndrome
Fibromyalgia is a common and chronic pain disorder that predominantly affects women. It belongs to the group of rheumatic disorders of the soft tissues, and is characterised by widespread chronic pain ... Musculoskeletal disease
H01637 Hypertriglyceridemia Hypertriglyceridemia (HTG) is a condition with fasting triglyceride (TG) levels in blood continuing to rise. HTG generally refers to an increase of plasma triglyceride (TG) concentrations above the 95th ... Endocrine and metabolic disease
H01638 Neuropathic pain
Neuralgia
Neuropathic pain is defined as pain caused by a lesion or disease affecting the somatosensory nervous system, and may be generated by either the peripheral or central nervous system, or both. It is especially ... Nervous system disease
H01639 Endometriosis Endometriosis is defined as the growth of the endometrial glands and stroma at extra-uterine sites, which are most commonly implanted over and under visceral and peritoneal surfaces within the female pelvis ... Reproductive system disease
H01640 Uterine leiomyoma
Fibroid
Uterine leiomyoma, also known as fibroid, is the most common benign neoplasm of the female genital tract. It is a discrete, round, firm, often multiple uterine tumor composed of smooth muscle and connective ... Reproductive system disease
H01641 Dry eye disease
Keratoconjunctivitis sicca
Dry eye disease (also called keratoconjunctivitis sicca) is multifactorial disease of the tears, lids, and ocular surface which can result in symptoms of discomfort and/or visual disturbance and/or tear ... Nervous system disease
H01642 Renal anemia Renal anemia is one of the most frequent complications of chronic kidney disease. Anemia leads to a decrease in oxygen delivery to vital organs, which is initially compensated for by tachycardia and cardiac ... Urinary system disease
H01643 Chilblains
Pernio
Chilblains, or pernio, is a localized inflammatory lesion of the skin resulting from an abnormal response to cold. It is characterized by persistent purple or purple-red nodules on acral skin, most commonly ... Immune system disease; Skin disease
H01644 Blepharitis Blepharitis is a chronic inflammatory condition of the eyelids associated with itchiness, redness, flaking, and crusting. It is among the most common ocular conditions affecting both children and adults ... Nervous system disease
H01645 Hyperthyroidism
Thyrotoxicosis
Hyperthyroidism is a pathological disorder characterised by increased thyroid hormone synthesis and secretion from the thyroid gland. The term thyrotoxicosis is not synonymous with hyperthyroidism. Thyrotoxicosis ... Endocrine and metabolic disease
1601 to 1640 of 3021 Prev 1 ... 36 37 38 39 40 41 42 43 44 45 46 ... 76 Next

[ KEGG | DISEASE | DRUG | MEDICUS ]