Number of the records: 1
Carneyho komplex
SYS d056733 LBL 00000nx--j2200000---45-- 005 20240119200625.8 100 $a 20100101asloy0103----ba0 152 $b mesh 250 $a Carneyho komplex $x BL $x CF $x CI $x CL $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $8 slo 300 1-
$a 2010 $8 eng 330 1-
$a Autosomal dominant syndrome characterized by cardiac and cutaneous MYXOMAS; LENTIGINOSIS (spotty pigmentation of the skin), and endocrinopathy and its associated endocrine tumors. The cardiac myxomas may lead to SUDDEN CARDIAC DEATH and other complications in Carney complex patients. The gene coding for the PRKAR1A protein is one of the causative genetic loci (type 1). A second locus is at chromosome 2p16 (type 2). $8 eng 450 $a Carney Complex, Type 2 $5 e $8 eng 450 $a Carney Complex, Type II $5 e $8 eng 450 $a Carney Myxoma-Endocrine Complex $5 e $8 eng 450 $a Carney Syndrome $5 e $8 eng 450 $a LAMB Syndrome $5 e $8 eng 450 $a Myxoma, Spotty Pigmentation, and Endocrine Overactivity $5 e $8 eng 450 $a NAME Syndrome $5 e $8 eng 450 $a Carneyho komplex, typ 2 $5 e $8 slo 450 $a Carneyho komplex typu II $5 e $8 slo 450 $a Carneyho myxóm-endokrinný komplex $5 e $8 slo 450 $a Carneyov syndróm $5 e $8 slo 450 $a LAMB syndróm $5 e $8 slo 450 $a myxóm, pigmentové škvrny a zvýšená endokrinná aktivita $5 e $8 slo 450 $a NAME syndróm $5 e $8 slo 686 $a C04.557.450.565.550.312 686 $a C04.588.894.309.500 686 $a C14.280.459.500 686 $a C16.131.077.229 686 $a C16.131.831.108 750 $a Carney Complex $8 eng 801 -0
$a SK $b BA006 $c 20100316 801 -0
$a SK $b BA006 $c 20100412 980 $x M
Number of the records: 1