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| Entry | Name | Description | Category | Pathway |
|---|---|---|---|---|
| H01405 | Lactococcus garvieae infection | Lactococcus garvieae, catalase-negative, facultative anaerobic cocci, is a major pathogen of fish and causes fatal hemorrhagic septicemia in fish such as yellowtail and trout, and it has also been isolated ... | Bacterial infectious disease | |
| H01406 | Streptococcus suis infection | Streptococcus suis, a Gram positive coccus, is a zoonotic pathogen that infects pigs and can occasionally cause serious infections in humans. The first case in humans was reported in Denmark in 1968. Human ... | Bacterial infectious disease | |
| H01407 | Capnocytophaga ochracea infection | Capnocytophaga ochracea is a Gram-negative bacterium, capnophilic (CO2-requiring) organism, originally isolated from a human oral cavity. C. ochracea is a normal inhabitant of the human mouth and other ... | Bacterial infectious disease | |
| H01408 | Periodontal disease | During the early stages of the periodontal disease, saccharolytic, aerobic Streptococcus spp. and other bacteria adhere to and colonize the tooth enamel and root surface. This sets the stage for Fusobacterium ... | Bacterial infectious disease | |
| H01409 | Methicillin-sensitive Staphylococcus aureus (MSSA) infection | Staphylococcus aureus is a Gram-positive human commensal bacterium persistently colonizing the anterior nares of about 30% of the human population. Methicillin-resistant S. aureus (MRSA) is known to have ... | Bacterial infectious disease | hsa05150 Staphylococcus aureus infection |
| H01410 | Anaerobic infection | Anaerobic infections are common and some are serious with a high mortality rate. The clinically important anaerobes are several genera of Gram-negative rods (Bacteroides, Prevotella, Porphyromonas, Fusobacterium ... | Bacterial infectious disease | |
| H01411 | Saccharomonospora viridis infection | Saccharomonospora viridis is the type species of the genus Saccharomonospora which belongs to the family Pseudonocardiaceae. Members of the species are frequently found in hot compost and hay, and its ... | Bacterial infectious disease | |
| H01412 | Perlman syndrome | Perlman syndrome is a rare autosomal recessive overgrowth disorder characterized by polyhydramnios with neonatal macrosomia, visceromegaly, distinctive facial appearance, renal dysplasia, nephroblastomatosis ... | Congenital malformation | |
| H01413 | Adams-Oliver syndrome | Adams-Oliver syndrome (AOS) is a rare condition defined by the combination of aplasia cutis congenita (ACC), characterized by scalp and skull lesions, and transverse limb abnormalities. Mutations in ARHGAP31 ... | Congenital malformation | |
| H01414 | Hafnia alvei infection | The genus Hafnia, a member of the family Enterobacteriaceae, is occasionally implicated in both intestinal and extraintestinal infections in humans. Hafnia alvei is a facultative anaerobic opportunistic ... | Bacterial infectious disease | |
| H01415 |
Donovanosis Granuloma inguinale |
Donovanosis (granuloma inguinale) is an acquired chronic, slowly progressive, mildly contagious disease caused by Klebsiella granulomatis that was called Calymmatobacterium granulomatis. This sexually ... | Bacterial infectious disease | |
| H01416 | Severe fever with thrombocytopenia syndrome | Severe fever with thrombocytopenia syndrome (SFTS) is a life-threatening infectious disease caused by SFTS virus (SFTSV), a phlebovirus in the order Bunyavirales of -ssRNA viruses, and transmitted by Ixodoidea ... | Viral infectious disease | |
| H01417 | Acute encephalitis | Acute encephalitis is a serious form of neurological disease caused by inflammation of the brain parenchyma. It is generally characterized by the acute onset of fever, altered mental status, new onset ... | Viral infectious disease; Nervous system disease | |
| H01418 |
Condyloma acuminatum Condylomata acuminata Genital warts |
Condyloma acuminatum is a sexually transmitted infection (STI) caused by the human papillomavirus (HPV). It is characterized by fleshy papules on the mucosa and skin of the anorectum and genitalia, with ... | Viral infectious disease | |
| H01419 | Middle East respiratory syndrome | Middle East respiratory syndrome (MERS) is a severe viral illness caused by Middle East respiratory syndrome coronavirus (MERS-CoV), a novel coronavirus that emerged in the Middle East in 2012. Since then ... | Viral infectious disease | |
| H01420 | Pharyngoconjunctival fever | Pharyngoconjunctival fever (PCF) is a syndrome attributed to human adenovirus B, particularly serotype 3, which causes small outbreaks, mainly among children. The syndrome may occur sporadically and can ... | Viral infectious disease | |
| H01421 | Acute hemorrhagic conjunctivitis | Acute hemorrhagic conjunctivitis (AHC) is a highly contagious viral conjunctivitis first observed in 1969 in Ghana. Causative agents thus far identified are enterovirus 70 and coxsackievirus A24 variant ... | Viral infectious disease | |
| H01422 | Carbapenem-resistant bacterial infection | Carbapenems [DG:DG01458] are a class of beta-lactam antibiotics often used as the last resort treatment for severe bacterial infections. Thus, the appearance of carbapenem resistance caused by acquisition ... | Bacterial infectious disease | |
| H01423 | Penicillin-resistant Streptococcus pneumoniae infection | Streptococcus pneumoniae is a common causative pathogen in community-acquired respiratory tract infections (RTIs), including acute otitis media, acute bacterial exacerbations of chronic bronchitis, acute ... | Bacterial infectious disease | |
| H01424 |
Group A streptococcal pharyngitis Group A streptococcal tonsillitis Group A streptococcal pharyngotonsillitis |
Group A streptococcal pharyngitis is an acute infection of the oropharynx and/or nasopharynx that is caused by group A streptococcus (Streptococcus pyogenes). Group A streptococcus is responsible for 5-15% ... | Bacterial infectious disease | |
| H01425 | Lysosomal storage disease | Lysosomal storage diseases (LSDs) are a group of inherited diseases that are characterised by the intracellular accumulation of incompletely degraded macromolecules. They result from a genetic defect in ... | Inherited metabolic disorder | |
| H01426 | Invasive streptococcal disease | Invasive streptococcal disease is defined as an infection associated with group A Streptococcus pyogenes. Since the mid-1980s, there have been reports from around the world of an increase in the incidence ... | Bacterial infectious disease | |
| H01427 | Mitochondrial disease | Mitochondrial diseases are clinically heterogeneous group of disorders that arise as a result of dysfunction of the mitochondria. They can be caused by mutation of genes encoded by either nuclear DNA or ... | Inherited metabolic disorder | |
| H01428 | Xeroderma pigmentosum | Xeroderma pigmentosum (XP) is a rare autosomal-inherited, skin and neurodegenerative disease in which exposure to sunlight can result in a high incidence of skin and mucous membrane cancer. XP is classified ... | Congenital malformation | |
| H01429 | Aseptic meningitis | Aseptic meningitis is one of the most common inflammatory disorders of the meninges and includes all types of meningitis not due to pyogenic bacteria. It has a very broad etiology, including both viral ... | Viral infectious disease; Nervous system disease | |
| H01430 | Viral gastroenteritis | Viral gastroenteritis is an infection of the stomach and intestines caused by a variety of viruses. Rotavirus, enteric adenovirus, calicivirus, and astrovirus typically cause diarrhea in infants and young ... | Viral infectious disease | |
| H01431 | Cushing syndrome | Cushing syndrome (CS) is a rare disorder resulting from prolonged exposure to excess glucocorticoids via exogenous and endogenous sources. The typical clinical features of CS are related to hypercortisolism ... | Endocrine and metabolic disease | hsa04934 Cushing syndrome |
| H01432 |
Choreoacanthocytosis Chorea-acanthocytosis |
Choreoacanthocytosis (CHAC) is a type of neuroacanthocytosis, a heterogeneous group of hereditary syndromes characterized by the association of neurologic abnormalities with acanthocytic red blood cells ... | Nervous system disease | |
| H01433 | Budd-Chiari syndrome | Budd-Chiari syndrome (BDCHS) is a heterogeneous group of disorders characterized by hepatic venous outflow obstruction at the hepatic veins or inferior vena cava. Clinically, the disease is characterized ... | Digestive system disease | |
| H01434 | Atypical hemolytic uremic syndrome | The haemolytic uraemic syndrome (HUS) is characterized by the triad of thrombocytopenia, microangiopathic haemolytic anaemia and acute renal failure. HUS may be classified as either diarrhoeal-associated ... | Hematologic disease | |
| H01435 | Congenital asplenia | Congenital asplenia is a rare developmental disorder that is characterized by the absence of a spleen at birth. The patients are prone to life-threatening bacterial infections. Isolated congenital asplenia ... | Congenital malformation | |
| H01436 | Guillain-Barre syndrome | Guillain-Barre syndrome (GBS) is an acute polyneuropathy characterized by progressive motor weakness of limbs with areflexia. This disease is usually triggered by an infection, which provokes immune-mediated ... | Nervous system disease | |
| H01437 |
Neurofibromatosis type 1 Von Recklinghausen disease |
Neurofibromatosis type 1 (NF1), also known as von Recklinghausen's disease, is an autosomal dominant disease caused by mutations of NF1 gene on chromosome 17. The NF1 gene encodes a RAS GTPase-activating ... | Congenital malformation | |
| H01438 | Neurofibromatosis type 2 | Neurofibromatosis 2 (NF2) is a rare autosomal dominant multiple neoplasia syndrome that is caused by inactivating mutations of the NF2 tumour suppressor gene. The course of the disease is usually progressive ... | Congenital malformation | |
| H01439 | Williams-Beuren syndrome | Williams-Beuren syndrome (WBS) is a rare autosomal dominant multisystem disorder associated with the hemizygous deletion of a number of genes on chromosome 7q11.23. The range of phenotypes may include ... | Chromosomal abnormality | |
| H01440 |
Acute necrotizing ulcerative gingivitis Vincent gingivitis Vincent angina Trench mouth |
Acute necrotizing ulcerative gingivitis, also known as Trench mouth, Vincent angina and Vincent gingivitis is an acute bacterial infection of the gingiva caused by spirochetes, fusiform bacteria, or an ... | Bacterial infectious disease | |
| H01441 | Pseudomonas aeruginosa infection | Pseudomonas aeruginosa is a leading cause of nosocomial bloodstream infections, ranking third among gram-negative bacteria, after Escherichia coli and Klebsiella species. Intrinsic resistance has been ... | Bacterial infectious disease | |
| H01442 |
Septic arthritis Pyogenic arthritis |
Septic arthritis is defined as a purulent infection in a joint cavity. The infection commonly reaches the joint in children by hematogenous spread or by direct extension of pathogenic bacteria. Staphylococcus ... | Bacterial infectious disease | |
| H01443 | Viridans group streptococcal infection | The viridans group streptococci (VGS), a heterogenous group of streptococcal species, are the predominant species of the human oral flora and commonly inhabit other areas of the upper respiratory, gastrointestinal ... | Bacterial infectious disease | |
| H01444 | Enterococcal infection | Enterococci are Gram-positive, catalase-negative, non-spore-forming, facultative anaerobic bacteria, which usually inhabit the alimentary tract of humans in addition to being isolated from environmental ... | Bacterial infectious disease |
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