Number of the records: 1
von Hippelova-Lindauova choroba
SYS d006623 LBL 00000cz--a2200000n--4500 005 20250606213106.1 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 $d BA006 $d BA006 065 $a C10.562.925 065 $a C14.907.077.925 065 $a C16.131.077.245.750 065 $a C16.320.184.750 066 $a 01 $c 03 150 $a von Hippelova-Lindauova choroba $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 Cerebelloretinal Angiomatosis, Familial $2 eng 450 $w v $a Lindau Disease $2 eng 450 $w v $a angiomatóza cerebeloretinálna familiárna $2 slo 450 $w v $a Lindauova choroba $2 slo 450 $w v $a Hippelova-Lindauova choroba $2 slo 450 $w v $a Hippel-Lindauova choroba $2 slo 450 $w v $a angiomatosis retinae $2 slo 450 $w v $a angiomatosis retinocerebellosa $2 slo 450 $w v $a von Hippelov-Lindauov syndróm $2 slo 450 $w v $a VHL syndróm $2 slo 665 $a 2008 (1975) $2 eng 680 9-
$i An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions. $2 eng 750 -2
$a von Hippel-Lindau Disease $2 eng 980 $x M
Number of the records: 1