Number of the records: 1
nezidioblastóza
SYS d046768 LBL 00000nz--a2200000o--4500 005 20250606215947.9 008 040707|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 065 $a C06.689.150.500 065 $a C16.614.200.500 065 $a C18.452.394.968.250.500 065 $a C18.452.394.984.200.500 066 $a 01 $c 03 150 $a nezidioblastóza $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 Hyperinsulinism, Familial, with Pancreatic Nesidioblastosis $2 eng 450 $w v $a hyperinzulinizmus familiárny, s nezidioblastózou pankreasu $2 slo 550 $7 sllk_us_auth*d018528 $Y ATP-Binding Cassette Transporters $w b $a ATP-viažuce kazetové transportéry 550 $7 sllk_us_auth*d018528 $Y ATP-Binding Cassette Transporters $w p $a ATP-viažuce kazetové transportéry 550 $7 sllk_us_auth*d054086 $Y KATP Channels $w p $a KATP kanály 665 $a 2005; use PANCREATIC DISEASES 1983-2004 $2 eng 665 $a Hyperinsulinism (1971-2004) $2 eng 665 $a Hyperplasia (1968-2004) $2 eng 665 $a Islets of Langerhans (1968-2004) $2 eng 680 9-
$i An inherited autosomal recessive syndrome characterized by the disorganized formation of new islets in the PANCREAS and CONGENITAL HYPERINSULINISM. It is due to focal hyperplasia of pancreatic ISLET CELLS budding off from the ductal structures and forming new islets of Langerhans. Mutations in the islet cells involve the potassium channel gene KCNJ11 or the ATP-binding cassette transporter gene ABCC8, both on CHROMOSOME 11. $2 eng 750 -2
$a Nesidioblastosis $2 eng 980 $x M
Number of the records: 1