Number of the records: 1
teleangiektázia dedičná hemoragická
SYS d013683 LBL 00000cz--a2200000n--4500 005 20250606214745.7 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 065 $a C14.907.454.900 065 $a C14.907.823.780 065 $a C15.378.463.515.900 065 $a C16.131.240.850.968 066 $a 01 $c 03 150 $a teleangiektázia dedičná hemoragická $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 Osler-Rendu Disease $2 eng 450 $w v $a Rendu-Osler-Weber Disease $2 eng 450 $w v $a Weber-Osler Disease $2 eng 450 $w v $a Weber-Osler Syndrome $2 eng 450 $w v $a teleangiektázia hereditárna hemoragická $2 slo 450 $w v $a Oslerova choroba $2 slo 450 $w v $a Oslerova-Renduova choroba $2 slo 450 $w v $a Oslerova-Renduova-Weberova choroba $2 slo 450 $w v $a Oslerova-Weberova-Renduova choroba $2 slo 450 $w v $a Renduova-Oslerova-Weberova choroba $2 slo 450 $w v $a teleangiektázia hereditárna hemoragická, typ 1 $2 slo 450 $w v $a Renduova-Oslerova-Weberova dedičná hemoragická teleangiektázia $2 slo 450 $w v $a Weberova-Oslerova choroba $2 slo 450 $w v $a Weberov-Oslerov syndróm $2 slo 550 $7 sllk_us_auth*d000798 $Y Angiomatosis $w b $a angiomatóza 665 $a 1968(1966); for OSLER-RENDU DISEASE use ANGIOMATOSIS 1963-1967 $2 eng 680 9-
$i An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA. $2 eng 750 -2
$a Telangiectasia, Hereditary Hemorrhagic $2 eng 980 $x M
Number of the records: 1