Number of the records: 1
Peutzov-Jeghersov syndróm
SYS d010580 LBL 00000cz--a2200000o--4500 005 20250606214614.7 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C04.700.633 065 $a C06.405.469.578.750 065 $a C16.320.700.667 065 $a C17.800.621.430.530.550.625 066 $a 01 $c 03 150 $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 $2 slo 450 $w v $a Lentiginosis, Perioral $2 eng 450 $w v $a lentiginopolyposis digestiva $2 slo 450 $w v $a lentiginóza periorálna $2 slo 450 $w v $a Peutzov-Tourainov syndróm $2 slo 665 $a 65; was see under POLYPI (now POLYPS) 1963-64 $2 eng 680 9-
$i 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. $2 eng 750 -2
$a Peutz-Jeghers Syndrome $2 eng 980 $x M
Number of the records: 1