Từ điển y khoa

Thuật ngữ y khoa chuẩn hóa theo MeSH, ICD-11, SNOMED CT.

62,341 terms indexed

• D002383Catalogs, Union as TopicMeSH

  Works about lists of books and other information sources held among a cooperating group of LIBRARIES.

• D002384CatalysisMeSH

  The facilitation of a chemical reaction by material (catalyst) that is not consumed by the reaction.

• D020134Catalytic DomainMeSH

  The region of an enzyme that interacts with its substrate to cause the enzymatic reaction.

• D002385CataplexyMeSH

  A condition characterized by transient weakness or paralysis of somatic musculature triggered by an emotional stimulus or physical exertion. Cataplexy is frequently associated with NARCOLEPSY. During a cataplectic attack, there is a marked reduction in muscle tone similar to the normal physiologic hypotonia that accompanies rapid eye movement sleep (SLEEP, REM). (From Adams et al., Principles of Neurology, 6th ed, p396)

• D002386CataractMeSH

  Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed)

• D002387Cataract ExtractionMeSH

  The removal of a cataractous CRYSTALLINE LENS from the eye.

• C563812Cataract, Age-Related Cortical, 1MeSH
• C563333Cataract, Age-Related NuclearMeSH
• C565815Cataract, Autosomal DominantMeSH

  Hereditary forms of cataract caused by mutations in the CRYAA gene. OMIM: 604219

• C565137Cataract, Autosomal Dominant NuclearMeSH
• C566909Cataract, Autosomal Dominant, Multiple Types 1MeSH

  mutation on phakinin

• C565136Cataract, Autosomal Recessive Congenital 1MeSH
• C567835Cataract, Autosomal Recessive Congenital 3MeSH

  aka CATC3

• C565298Cataract, Autosomal Recessive, Early-Onset, PulverulentMeSH
• C565301Cataract, Central Saccular, With Sutural OpacitiesMeSH
• C563728Cataract, Congenital Nuclear, Autosomal Recessive 1MeSH
• C565725Cataract, Congenital Nuclear, Autosomal Recessive 2MeSH
• C566923Cataract, Congenital Nuclear, Autosomal Recessive 3MeSH
• C563435Cataract, Congenital Zonular, with Sutural OpacitiesMeSH
• C563294Cataract, Congenital, Cerulean Type, 2MeSH
• C563819Cataract, Congenital, Cerulean Type, 3MeSH
• C564353Cataract, Congenital, with Mental Impairment and Dentate Gyrus AtrophyMeSH
• C565133Cataract, Coppock-LikeMeSH
• C563604Cataract, Cortical Pulverulent, Late-OnsetMeSH
• C566955Cataract, Cortical, Juvenile-OnsetMeSH

  mutation on filensin

• C566162Cataract, Crystalline AculeiformMeSH
• C566161Cataract, Crystalline CoralliformMeSH
• C566160Cataract, FloriformMeSH
• C567434Cataract, Juvenile, With Microcornea And GlucosuriaMeSH

  mutation on Monocarboxylate transporter 12

• C566481Cataract, Lamellar 2MeSH
• C566861Cataract, Microcephaly, Arthrogryposis, Kyphosis SyndromeMeSH
• C566157Cataract, Nuclear Diffuse NonprogressiveMeSH
• C564596Cataract, Nuclear ProgressiveMeSH
• C566156Cataract, Nuclear TotalMeSH
• C563603Cataract, Polymorphic and LamellarMeSH
• C565134Cataract, Posterior Polar, 2MeSH
• C565130Cataract, Progressive Polymorphic CorticalMeSH
• C563426Cataract, PulverulentMeSH
• C565703Cataract, Pulverulent, Juvenile-OnsetMeSH

  mutation on MAF

• C565131Cataract, Punctate, Progressive Juvenile-OnsetMeSH
• C564619Cataract, Sutural, with Punctate and Cerulean OpacitiesMeSH
• C565132Cataract, Variable Zonular PulverulentMeSH
• C565135Cataract, Zonular Central NuclearMeSH
• C566158Cataract, Zonular Pulverulent 1MeSH

  mutation on GJA8

• C566608Cataract, Zonular Pulverulent 3MeSH

  mutation on GJA3

• C563390Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental RetardationMeSH
• D051079CatarrhiniMeSH

  An infraorder of PRIMATES comprised of the families CERCOPITHECIDAE (old world monkeys); HYLOBATIDAE (siamangs and GIBBONS); and HOMINIDAE (great apes and HUMANS). With the exception of humans, they all live exclusively in Africa and Asia.

• D002388Catastrophic IllnessMeSH

  An acute or prolonged illness usually considered to be life-threatening or with the threat of serious residual disability. Treatment may be radical and is frequently costly.

• D058443CatastrophizationMeSH

  Cognitive and emotional processes encompassing magnification of pain-related stimuli, feelings of helplessness, and a generally pessimistic orientation.

• D002389CatatoniaMeSH

  A neuropsychiatric disorder characterized by one or more of the following essential features: immobility, mutism, negativism (active or passive refusal to follow commands), mannerisms, stereotypies, posturing, grimacing, excitement, echolalia, echopraxia, muscular rigidity, and stupor; sometimes punctuated by sudden violent outbursts, panic, or hallucinations. This condition may be associated with psychiatric illnesses (e.g., SCHIZOPHRENIA; MOOD DISORDERS) or organic disorders (NEUROLEPTIC MALIGNANT SYNDROME; ENCEPHALITIS, etc.). (From DSM-IV, 4th ed, 1994; APA, Thesaurus of Psychological Index Terms, 1994)