Number of the records: 1
Peutzov-Jeghersov syndróm
SYS d010580 LBL 00000cx--j22000003--45-- 005 20240119195901.7 100 $a 19990101csloy0103----ba0 152 $b mesh 250 $a Peutzov-Jeghersov syndróm $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 65; was see under POLYPI (now POLYPS) 1963-64 $8 eng 330 1-
$a A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits. $8 eng 450 $a Lentiginosis, Perioral $5 e $8 eng 450 $a lentiginopolyposis digestiva $5 e $8 slo 450 $a lentiginóza periorálna $5 e $8 slo 450 $a Peutzov-Tourainov syndróm $5 e $8 slo 686 $a C04.700.633 686 $a C06.405.469.578.750 686 $a C16.320.700.667 686 $a C17.800.621.430.530.550.625 750 $a Peutz-Jeghers Syndrome $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20020627 980 $x M
Number of the records: 1