Medical dictionary

Medical terminology normalized via MeSH, ICD-11, SNOMED CT.

62,341 terms indexed

• L02.11Cutaneous abscess of neckICD-10-CM
• L02.818Cutaneous abscess of other sitesICD-10-CM
• L02.215Cutaneous abscess of perineumICD-10-CM
• L02.411Cutaneous abscess of right axillaICD-10-CM
• L02.611Cutaneous abscess of right footICD-10-CM
• L02.511Cutaneous abscess of right handICD-10-CM
• L02.415Cutaneous abscess of right lower limbICD-10-CM
• L02.413Cutaneous abscess of right upper limbICD-10-CM
• L02.219Cutaneous abscess of trunk, unspecifiedICD-10-CM
• L02.216Cutaneous abscess of umbilicusICD-10-CM
• L02.619Cutaneous abscess of unspecified footICD-10-CM
• L02.519Cutaneous abscess of unspecified handICD-10-CM
• L02.91Cutaneous abscess, unspecifiedICD-10-CM
• A06.7Cutaneous amebiasisICD-10-CM
• A44.1Cutaneous and mucocutaneous bartonellosisICD-10-CM
• A22.0Cutaneous anthraxICD-10-CM
• L30.2Cutaneous autosensitizationICD-10-CM
• B40.3Cutaneous blastomycosisICD-10-CM
• B43.0Cutaneous chromomycosisICD-10-CM
• B38.3Cutaneous coccidioidomycosisICD-10-CM
• B45.2Cutaneous cryptococcosisICD-10-CM
• A36.3Cutaneous diphtheriaICD-10-CM
• A26.0Cutaneous erysipeloidICD-10-CM
• B55.1Cutaneous leishmaniasisICD-10-CM
• A32.0Cutaneous listeriosisICD-10-CM
• D47.01Cutaneous mastocytosisICD-10-CM
• B46.3Cutaneous mucormycosisICD-10-CM
• A31.1Cutaneous mycobacterial infectionICD-10-CM
• B87.0Cutaneous myiasisICD-10-CM
• A43.1Cutaneous nocardiosisICD-10-CM
• B78.1Cutaneous strongyloidiasisICD-10-CM
• C565129Cutis Gyrata Syndrome of Beare And StevensonMeSH

  mutation in FGFR2

• D003483Cutis LaxaMeSH

  A group of connective tissue diseases in which skin hangs in loose pendulous folds. It is believed to be associated with decreased elastic tissue formation as well as an abnormality in elastin formation. Cutis laxa is usually a genetic disease, but acquired cases have been reported. (From Dorland, 27th ed)

• C567716Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary AbnormalitiesMeSH

  LTBP4 mutations

• C562627Cutis Laxa, Autosomal DominantMeSH

  PROM mutation in elastin

• C562628Cutis Laxa, Autosomal Recessive, Type IMeSH
• C562632Cutis Laxa, Autosomal Recessive, Type IIAMeSH

  PROM mutation in ATP6V0A2 gene

• C567855Cutis Laxa, Autosomal Recessive, Type IIBMeSH

  mutation in PYCR1

• C563639Cutis Laxa-Marfanoid SyndromeMeSH
• C565661Cutis Verticis Gyrata and Mental DeficiencyMeSH
• C565306Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural DeafnessMeSH
• L57.4Cutis laxa senilisICD-10-CM
• L57.2Cutis rhomboidalis nuchaeICD-10-CM
• C574098Cv-d protein, DrosophilaMeSH

  a vitellogenin-like lipoprotein that binds bone morphogenetic protein; RefSeq NM_169676

• C575007CvfA endoribonuclease, Streptococcus pyogenesMeSH

  a membrane-associated, required for the thermoregulation of capsule synthesis

• C577095Cxcl3 protein, mouseMeSH

  GenBank AY311403

• C572517Cy-N(3) fluorescent probeMeSH

  structure in first source

• C561397CyNE 2-DGMeSH

  a fluorescent dye for cancer imaging; structure in first source

• C561222CyNE790MeSH

  a fluorescent NIR-protein labeling dye; structure in first source

• D031293CyamopsisMeSH

  A plant genus of the family FABACEAE that is the source of guar gum.