ENTITY
stringlengths 8
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| DEFINITION
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8.47k
⌀ | ALIASES
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13.6k
⌀ | NAME
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1.98k
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C1022433 | null | Trachypaninae | Trachypachidae |
C1301931 | The time of day it is determined or presumed that an individual has died. | Time of death|Time of Death|death time|Time of death (observable entity)|time of death | Time of death |
C1516248 | An elaboration of a sequence of biological or biochemical events that play a role in the metabolism of carbohydrates. | Carbohydrate Metabolism - Reference Pathway | Carbohydrate Metabolism Pathway |
C3767455 | null | Achromobacter pulmonis (organism)|Achromobacter pulmonis|Achromobacter genogroup 11 | Achromobacter pulmonis |
C1922455 | null | Dendrocopos medius (organism)|Dendrocoptes medius|Leiopicus medius|Middle spotted woodpecker|Dendrocopos medius|Picoides medius | Dendrocopos medius |
C0323487 | null | Hyalomma anatolicum (organism)|Hyalomma anatolicum|Hyalomma excavatum | Hyalomma anatolicum |
C1159762 | The process in which a microorganism (or other particulate material) is rendered more susceptible to phagocytosis by coating with an opsonin, a blood serum protein such as a complement component or antibody. [GOC:add, GOC:mah, ISBN:0198506732, ISBN:068340007X, ISBN:0781735149] | null | opsonization |
C1621719 | A variant of peripheral T-cell lymphoma, not otherwise specified. It is characterized by the presence of neoplastic small lymphocytes infiltrating the lymph nodes in a diffuse and less frequently interfollicular pattern. There is an associated proliferation of epithelioid histiocytes forming confluent clusters. | Lennert's Variant Peripheral T-Cell Lymphoma|Lennert Variant Peripheral T-Cell Lymphoma|Lymphoepithelioid Variant Peripheral T-Cell Lymphoma|Lennert lymphoma|Lennert Lymphoma|Lymphoepithelioid lymphoma|lennerts lymphoma|Lymphoepithelioid Cell Variant Peripheral T-Cell Lymphoma|Lennert's lymphoma|Lymphoepithelioid lymphoma (disorder)|Lennert's Lymphoma | Lymphoepithelioid lymphoma (clinical) |
C1456496 | null | Brain damage|Traumatic AND/OR non-traumatic brain injury (disorder)|Traumatic AND/OR non-traumatic brain injury | Traumatic AND/OR non-traumatic brain injury |
C0029218 | A measurement of the heaviness of a body organ. | Organ Weight|organ weights|Organ weight|Weight, Organ|Organ weight (finding)|organ weight|organs weights | Organ Weight |
C1336861 | A carcinoma with poor prognosis that arises from the pancreas. It is characterized by the presence of a significant malignant component that does not show differentiation. The malignant cells represent a mixture of large, pleomorphic cells and giant cells, or adenocarcinoma cells and spindle cells, or spindle cells. | Pleomorphic Large Cell Pancreatic Carcinoma|Undifferentiated (Anaplastic) Pancreatic Carcinoma|Sarcomatoid Pancreatic Carcinoma|Pancreatic Carcinosarcoma|Undifferentiated Carcinoma of the Pancreas|Undifferentiated Pancreatic Carcinoma|Undifferentiated Carcinoma of Pancreas|Spindle Cell Pancreatic Carcinoma | Undifferentiated Pancreatic Carcinoma |
C1823355 | null | EMC6|EMC6 gene|ER membrane protein complex subunit 6|MGC2963|RAB5IFL | EMC6 gene |
C1823355 | null | EMC6|EMC6 gene|ER membrane protein complex subunit 6|MGC2963|RAB5IFL | EMC6 gene |
C0682747 | null | class I alcohol dehydrogenase isoenzyme | class I ADH isoenzyme |
C1463606 | null | Borrelia turcica|Borrelia turcica (organism) | Borrelia turcica |
C0205828 | A lymphangioma characterized by the presence of thin-walled cavernous lymphatic spaces. | Cavernous lymphangioma (morphologic abnormality)|LYMPHANGIOMA, CAVERNOUS|Cavernous lymphangioma|Lymphangioma, Cavernous|Cavernous Lymphangioma|Cavernous Lymphangiomas|Lymphangiomas, Cavernous | Cavernous lymphangioma |
C3268725 | null | metacaspase activity | metacaspase activity |
C4235287 | The multiplication or reproduction of vascular smooth muscle cells, resulting in the expansion of a cell population. A vascular smooth muscle cell is a non-striated, elongated, spindle-shaped cell found lining the blood vessels. [PMID:23246467] | VSMC proliferation | vascular smooth muscle cell proliferation |
C4572776 | null | null | Bovine picobirnavirus |
C0266214 | null | Congenital rectal stenosis|Congenital rectal stricture|Congenital stricture of rectum|Congenital stricture of rectum (disorder) | Congenital stricture of rectum |
C4053958 | Systemic lupus erythematosus nephritis exhibiting mesangial hypercellularity or mesangial expansion by light microscopy, with mesangial immune deposits. Isolated subepithelial or subendothelial deposits may be visible by immunofluorescence or electron microscopy, but not by light microscopy. (Weening, Jan J. et al. (2004). The Classification of Glomerulonephritis in Systemic Lupus Erythematosus Revisited. Journal of the American Society of Nephrology 15(2), 241-50.) | Mesangial Proliferative Lupus Nephritis|Systemic Lupus Erythematosus Nephritis Class II | Systemic Lupus Erythematosus Nephritis Class II |
C4517412 | null | Zero point zero six|0.06 (qualifier value) | 0.06 |
C1071338 | null | Mycobacteriophage Bxb1|Mycobacterium phage Bxb1 | Mycobacterium virus Bxb1 |
C0023439 | A rare acute myeloid leukemia characterized by abnormal EOSINOPHILS in the bone marrow. | Leukemia, Acute Eosinophilic|Acute eosinophilic leukemia|Acute eosinophilic leukaemia|Acute Eosinophilic Leukemia|Acute eosinophilic leukemia (disorder)|Eosinophilic Leukemias, Acute|Eosinophilic Leukemia, Acute|Leukemia, Eosinophilic, Acute|Acute Eosinophilic Leukemias|Leukemias, Acute Eosinophilic | Leukemia, Eosinophilic, Acute |
C0023439 | A rare acute myeloid leukemia characterized by abnormal EOSINOPHILS in the bone marrow. | Leukemia, Acute Eosinophilic|Acute eosinophilic leukemia|Acute eosinophilic leukaemia|Acute Eosinophilic Leukemia|Acute eosinophilic leukemia (disorder)|Eosinophilic Leukemias, Acute|Eosinophilic Leukemia, Acute|Leukemia, Eosinophilic, Acute|Acute Eosinophilic Leukemias|Leukemias, Acute Eosinophilic | Leukemia, Eosinophilic, Acute |
C0258708 | null | lysine clonixinate|clonixinate lysine|L-Lysine, mono(2-((3-chloro-2-methylphenyl)amino)-3-pyridinecarboxylate)|lysine clonixin | lysine clonixinate |
C1412668 | null | ATP5PF|ATP5J|MITOCHONDRIAL ATP SYNTHASE, SUBUNIT F6|ATP5PF gene|MITOCHONDRIAL ATP SYNTHASE, COUPLING FACTOR 6|CF6|ATP synthase peripheral stalk subunit F6|ATP5|ATP SYNTHASE, H+ TRANSPORTING, MITOCHONDRIAL FO COMPLEX, SUBUNIT F6|coupling factor 6 | ATP5PF gene |
C0602210 | null | alpha-phellandrene|p-mentha-1,5-diene|5-isopropyl-2-methyl-1,3-cyclohexadiene | alpha phellandrene |
C0254211 | null | UMIFENOVIR|1-methyl-2-((phenylthio)methyl)-3-carbethoxy-4-((dimethylamino)methyl)-5-hydroxy-6-bromindole hydrochloride|arbidol|arbidole|Umifenovir|umifenovir | arbidol |
C0730547 | null | Advice about HIV prevention|Human immunodeficiency virus prevention education|Human immunodeficiency virus prevention education (procedure) | HIV prevention education |
C0291575 | null | dual leucine zipper bearing kinase|mitogen-activated protein kinase kinase kinase 12|protein kinase MUK|MAPK-upstream kinase|zipper (leucine) protein kinase|MAP kinase upstream kinase|MUK protein kinase | mitogen-activated protein kinase kinase kinase 12 |
C1852551 | A rare form of superficial corneal dystrophy with recurrent episodes of epithelial erosions from childhood in the absence of associated diseases. The erosions begin spontaneously or are precipitated by minor trauma, dust or smoke. The condition may become apparent by 6 months of age, but as a rule it only starts at 4 to 6 years of age. Most patients have attacks of redness, photophobia, epiphora, and ocular pain. Some experience a burning sensation and report sensitive eyes for years. Vision is sometimes impaired. Autosomal dominant pattern of inheritance. | EPITHELIAL RECURRENT EROSION DYSTROPHY|Dystrophia Smolandiensis|Epithelial recurrent erosion dystrophy of cornea (disorder)|Corneal Erosions, Recurring Hereditary|CORNEAL EROSIONS, RECURRING HEREDITARY|ERED|Recurrent hereditary corneal erosions|Dystrophia Helsinglandica|Epithelial recurrent erosion dystrophy of cornea|Epithelial recurrent erosion dystrophy | Epithelial Recurrent Erosion Dystrophy |
C4539942 | null | FIBROMATOSIS, GINGIVAL, 5|GINGF5|GGF5|FIBROMATOSIS, GINGIVAL, HEREDITARY, 5|HGF5 | FIBROMATOSIS, GINGIVAL, 5 |
C1283248 | null | Cutting - action (qualifier value) | Cutting - action |
C1283248 | null | Cutting - action (qualifier value) | Cutting - action |
C5137287 | A protein-containing complex that monoubiquitinates histone H2A on K119, thus it facilitates the maintenance of the transcriptionally repressive state of some genes, such as BCL6. It consists of the corepressor BCOR or BCORL1, a Polycomb group (PcG) and a SCF ubiquitin ligase subcomplexes.nIn mammals, the core subunits of the complex include the PcG and PcG-associated proteins NSPC1, RING1, RNF2, and RYBP and the components of the SCF ubiquitin ligase, SKP1, and FBXL10. [PMID:16943429, PMID:22325352, PMID:24515802] | BCOR/BCORL1 complex|non-canonical BCOR-PRC1.1 complex|non-canonical BCOR-PRC1.1 complex location|non-canonical PRC1-BCOR complex|non-canonical PRC1-BCOR complex location|BCL6 corepressor (BCOR) complex location|BCOR complex location|BCL6 corepressor (BCOR) complex|PRC1.1 complex location|BCOR/BCORL1 complex location|PRC1.1 complex | BCOR complex |
C4693860 | null | CHUJANS|CHUNG-JANSEN SYNDROME|DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHISM|DIDOD | CHUNG-JANSEN SYNDROME |
C1151633 | Catalysis of the reaction: pyruvate + lipoamide = S-acetyldihydrolipoamide + CO2. [EC:1.2.4.1] | quinone-dependent pyranose dehydrogenase activity|PDH|pyranose-quinone oxidoreductase activity|pyruvate:dihydrolipoyllysine-residue acetyltransferase-lipoyllysine 2-oxidoreductase (decarboxylating, acceptor-acetylating)|pyranose dehydrogenase (acceptor) activity|pyranose dehydrogenase activity|pyruvate dehydrogenase (lipoamide) activity|pyranose:acceptor oxidoreductase activity|pyruvate dehydrogenase (acetyl-transferring) activity|pyruvate:lipoamide 2-oxidoreductase (decarboxylating and acceptor-acetylating) activity | pyruvate dehydrogenase (lipoamide) activity |
C0324180 | null | pony|Pony, NOS|Pony (organism) | Pony |
C1428467 | null | FAM71E2|FAM71E2 gene|family with sequence similarity 71 member E2|DKFZp434G1729 | FAM71E2 gene |
C1428467 | null | FAM71E2|FAM71E2 gene|family with sequence similarity 71 member E2|DKFZp434G1729 | FAM71E2 gene |
C1455205 | null | (R)-lavandulyl (S)-2-methylbutanoate|lavandulyl-2-methylbutanoate|lavandulyl 2-methylbutanoate | 2-isopropenyl-5-methyl-4-hexenyl 2-methylbutanoate |
C1455205 | null | (R)-lavandulyl (S)-2-methylbutanoate|lavandulyl-2-methylbutanoate|lavandulyl 2-methylbutanoate | 2-isopropenyl-5-methyl-4-hexenyl 2-methylbutanoate |
C4305142 | null | Borrelia bavariensis (organism)|Borreliella bavariensis|Borrelia bavariensis|Borrelia sp. PFek|Borrelia garinii OSPA serotype 4 | Borreliella bavariensis |
C1192375 | null | null | Toxolasma |
C1016648 | null | null | Ptychobranchus |
C1016642 | null | null | Medionidus |
C1090431 | null | null | Obovaria |
C1044258 | null | null | Epioblasma |
C1930782 | null | null | Hamiota |
C4310715 | null | TROFAS|THAUVIN-ROBINET-FAIVRE SYNDROME | THAUVIN-ROBINET-FAIVRE SYNDROME |
C3672369 | null | Dwarf brocket|Mazama chunyi|Mazama chunyi (organism) | Mazama chunyi |
C2787473 | null | null | Parmarion martensi |
C4539436 | null | null | Low aldosterone level |
C3763125 | null | null | Scartichthys |
C2935938 | null | null | Ossix |
C1073093 | null | null | Asphondylia |
C3985909 | null | Brahmophthalma hearseyi | Brahmaea hearseyi |
C1083287 | null | null | Diabrotica |
C1006945 | null | null | Pyraloidea |
C0524658 | null | Giant Silkworms|Giant Silkworm|Silkworm, Giant | Silkworms, Giant |
C0061104 | A cell surface antigen expressed on all tumors of neuroectodermal origin, including melanoma, neuroblastomas, sarcoma, astrocytomas, and small cell lung cancer. GD2, an O-acetylated disialoganglioside, belongs to the group of glycosphingolipids that are widely expressed in many tissues and organs in vertebrates and have been suggested to be involved in the regulation of development and differentiation as recognition molecules or signal modulators. Due to its high level of expression in neuroblastoma, GD2 has the potential to be used as a component of anti-neuroblastoma vaccines, in addition to being used in polyvalent anti-melanoma vaccines. | Disialylganglioside GD2|GD2-ganglioside (substance)|GD2-ganglioside|ganglioside GD2|Ganglioside GD2|GD2 ganglioside|GalNAc(beta 1->4)-[NeuAc(alpha 2->8)NeuAc(alpha 2->3)]Gal(beta 1->4)GlcCer | ganglioside, GD2 |
C1156524 | The anaerobic chemical reactions and pathways resulting in the breakdown of glycerol, yielding energy in the form of ATP. [GOC:mah] | glycerol fermentation | anaerobic glycerol catabolic process |
C2327741 | null | Area orbitalis externa|Brodmann area 10|Lateral orbital area|BA10|Area 10 of Brodmann | Brodmann area 10 |
C0428696 | null | Relative humidity|Relative humidity (observable entity) | Relative humidity |
C0998444 | null | Chloridea | Heliothis |
C1553338 | Denotes the inhabitants of Dominica, a person from there, or their descendants elsewhere. | Dominica Islander|DOMINICA ISLANDER|Dominican | Dominica Islander race |
C3653553 | null | null | SELECTIVE CALCIUM CHANNEL BLOCKERS WITH MAINLY VASCULAR EFFECTS |
C3653553 | null | null | SELECTIVE CALCIUM CHANNEL BLOCKERS WITH MAINLY VASCULAR EFFECTS |
C4023390 | Absence of the cochlea, a spiral shaped cavity in the inner ear, owing to a developmental defect. [HPO:dfitzpatrick] | Absent cochlea | Cochlear aplasia |
C0344485 | null | Intradural spinal arachnoid cyst|SPINAL INTRADURAL ARACHNOID CYSTS|Arachnoid cysts, spinal intradural|Intradural spinal arachnoid cyst (disorder) | Spinal intradural arachnoid cysts |
C0672377 | null | null | polyguluronate |
C4090381 | null | null | Eupentacta fraudatrix |
C2000926 | null | null | palythine |
C0035331 | A carotenoid constituent of visual pigments. It is the oxidized form of retinol which functions as the active component of the visual cycle. It is bound to the protein opsin forming the complex rhodopsin. When stimulated by visible light, the retinal component of the rhodopsin complex undergoes isomerization at the 11-position of the double bond to the cis-form; this is reversed in "dark" reactions to return to the native trans-configuration. | retinaldehyde|Aldehyde, Vitamin A|retinene|RETINAL, ALL-TRANS|Retinyl Aldehyde|retinal (bacteriorhodopsin)|Retinaldehyde (substance)|Retinene|Vitamin A Aldehyde|Retinal|retinal|Axerophthal|Retinaldehyde | Retinaldehyde |
C0032863 | The exertion of a strong influence or control over others in a variety of settings--administrative, social, academic, etc. | Powers, Psychological|power [a psychology concept]|power|powered|powers|Power|Power (Psychology)|Power, Psychological|Psychological Power|Psychological Powers | Power (Psychology) |
C1180063 | null | flagellar axoneme|Flagellum axoneme|Axoneme of flagellum|flagellum axoneme | Axoneme of flagellum |
C0324079 | null | Nellore cow|Nelore cattle|Nelore cattle breed (organism)|Nellore cattle breed (organism)|Nellore cattle breed|Nelore cattle breed | Nellore cattle |
C1823587 | null | UBX DOMAIN-CONTAINING PROTEIN 8|UBX domain protein 3B|UBXN3B|KIAA0887|UBXD8|FAF2|FAF2 gene|Fas associated factor family member 2|ETEA|FAF FAMILY, MEMBER 2|EXPRESSED IN T CELLS AND EOSINOPHILS IN ATOPIC DERMATITIS|expressed in T cells and eosinophils in atopic dermatitis|FAS-ASSOCIATED FACTOR FAMILY, MEMBER 2 | FAF2 gene |
C1823587 | null | UBX DOMAIN-CONTAINING PROTEIN 8|UBX domain protein 3B|UBXN3B|KIAA0887|UBXD8|FAF2|FAF2 gene|Fas associated factor family member 2|ETEA|FAF FAMILY, MEMBER 2|EXPRESSED IN T CELLS AND EOSINOPHILS IN ATOPIC DERMATITIS|expressed in T cells and eosinophils in atopic dermatitis|FAS-ASSOCIATED FACTOR FAMILY, MEMBER 2 | FAF2 gene |
C1417318 | null | mental retardation, X-linked 73|MRX73 gene|MRX73 | MRX73 gene |
C1417318 | null | mental retardation, X-linked 73|MRX73 gene|MRX73 | MRX73 gene |
C0080517 | null | PiLPC | 1-palmitoyl-2-isolinoleoyl phosphatidylcholine |
C0238596 | null | CORTICOTROPIN, DECREASED|ACTH, DECREASED | ADRENOCORTICOTROPIC HORMONE, DECREASED |
C2215935 | An electrocardiographic finding of complete failure of atrial electrical impulse conduction to the ventricles. This is manifested on the ECG by disassociation of atrial and ventricular rhythms. The atrial rate must be faster than the ventricular rate. (CDISC) | Third Degree Atrioventricular Block|3rd Degree Heart Block|3RD DEGREE AV BLOCK|AV Block Third Degree by EKG Finding|AV block, complete (third-degree)|Third Degree AV Block|Complete AV Block|AV Block Third Degree|Complete Heart Block|AV Block Third Degree by ECG Finding | Electrocardiogram atrioventricular block complete heart block |
C0149491 | null | 1-Piperazineethanol, 4-(3-(2-chloro-9H-thioxanthen-9-ylidene)propyl)-, 1-acetate|Zuclopenthixol acetate|zuclopenthixol acetate|(Z)-4-[3-(2-chlorothioxanthen-9-ylidene)propyl]-1-piperazineethanol Acetate|Zuclopenthixol Acetate|Zuclopenthixol acetate (substance)|ZUCLOPENTHIXOL ACETATE|clopenthixol acetate ester|(Z)-4-(3-(2-chlorothioxanthen-9-ylidene)propyl)-1-piperazineethanol acetate | zuclopenthixol acetate |
C3641874 | Cone beam computed tomography that includes megavoltage images. | Cone Beam Megavoltage Imaging|megavoltage computed tomography|Megavoltage Computed Tomography|Cone Beam Megavoltage CT Imaging|Megavoltage Cone Beam Computed Tomography|MV Cone Beam CT|Cone Beam Megavoltage Computed Tomography|MVCT|Cone Beam Megavoltage Computed Tomography Imaging|Cone Beam Megavoltage CT | Megavoltage Cone Beam Computed Tomography |
C1443927 | null | Sheep blood agar (substance) | Sheep blood agar |
C1034627 | null | null | Idris |
C3687785 | null | Cloacal swab | Cloacal swab (specimen) |
C1679912 | null | null | Schistocerca cancellata |
C1503848 | null | Hemiramphus buffonis | Zenarchopterus buffonis |
C1503848 | null | Hemiramphus buffonis | Zenarchopterus buffonis |
C1532132 | null | Length of vessel segment (observable entity)|Length of vessel segment | Length of segment |
C1646658 | null | null | Mylabris variabilis |
C2643850 | null | null | Goniopora columna |
C3826394 | null | null | Epilepsy in children |
C4631930 | null | null | Mammaria |
C2245791 | The portion of the plasma membrane surrounding a dendritic spine. [GOC:mah] | null | dendritic spine membrane |
C0369833 | null | Saturated phosphatidylcholine (substance) | Saturated phosphatidylcholine |
Subsets and Splits