CCA

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Related to FBN2: FBN3

CCA

(1) (Common Cryptographic Architecture) Cryptography software from IBM for MVS and DOS applications.

(2) (Compatible Communications Architecture) A Network Equipment Technology protocol for transmitting asynchronous data over X.25 networks.
References in periodicals archive ?
On the first case, there was no gross chromosomal rearrangement on the long arm of chromosome 5, where the APC and FBN2 genes were located.
Caracteristicas del sindrome de Marfan y otros diagnosticos diferenciales Diagnostico diferencial Genes con mutaciones Patron conocidas hereditario SM FBN1 AD Homocistinuria clasica CBS AR (tipo 1) (6) Sindrome de tortuosidad SLC2A10 AD arterial Aracnodactilia FBN2 AD contractural congenita Sindrome de Stickler (7) COL2A1-COL11A1 y COLllA2 AD Sindrome de Lujan-Fryns Desconocido RLX (8) Sindrome de Achard Desconocido AD Fenotipo MASS FBN1 AD Sindrome de Loeys-Dietz TGFBR1/2 AD Sindrome de Ehlers Danlos COL3A1, COL1A2, PLOD) AD tipos IV, VI, VII Sindrome de FBN1 AD Shprintzen-Goldberg Sindrome de aneurisma y TGFBR1/2 ACTA2 FBN1 MYH11 AD diseccion aortica toracica familiar Sindrome de prolapso de No se conoce un AD la valvula mitral (9) gen especifico.
11] APP, COL14A1, ROBO1, ITGAV, COL12A1, SCARB1, SCARB2, CNTN3, MFAP4, COL24A1, THBS2 multicellular 46 AEBP1, S100A6, HUS1, UTRN, 0,005 organismal GPM6B, POSTN, FKBP1A, ENPEP, development MYLIP, CBFB, PTK2, APP, ROBO1, CASP7, ITGAV, COL12A1, FBN2, LOX, USH2A, OLFM1, DCLK1, MLLT3, EGFL6, NRXN3, MAP1B, CHODL, ITGA2, AFF3, IGF2, SIRT1, COL5A1, CTNNBIP1, DKK3, MAN2A1, DACT1, CNTF, TMEM111, SFRP2, GRN, IRF1, SORT1, CNTN3, PSME4, COL1A1, CASQ2, MYH10 muscle organ 8 APP, AEBP1, CNTF, UTRN, CHODL, 0,008 development FKBP1A, SIRT1, MYH10 lipid 9 PTGES3, SAMD8, CYB5R1, AGPAT5, 0,026 biosynthetic C1QTNF3, LASS3, ALOX5AP, process SCARB1, ELOVL6 La interpretacion funcional mostro enriquecimiento en funciones estrechamente relacionadas con el desarrollo y adipogenesis del tejido muscular.