Počet záznamov: 1
piebaldizmus
SYS d016116 LBL 00000cx--j22000003--45-- 005 20240119201332.3 100 $a 19920606csloy0103----ba0 152 $b mesh 250 $a piebaldizmus $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 91 $8 eng 300 1-
$a Albinism (1966-1971) $8 eng 300 1-
$a Pigmentation Disorders (1966-1990) $8 eng 330 1-
$a Autosomal dominant, congenital disorder characterized by localized hypomelanosis of the skin and hair. The most familiar feature is a white forelock presenting in 80 to 90 percent of the patients. The underlying defect is possibly related to the differentiation and migration of melanoblasts, as well as to defective development of the neural crest (neurocristopathy). Piebaldism may be closely related to WAARDENBURG SYNDROME. $8 eng 450 $a Albinism, Cutaneous $5 e $8 eng 450 $a Albinism, Partial $5 e $8 eng 450 $a pieboldizmus $5 e $8 slo 450 $a albinizmus ohraničený $5 e $8 slo 450 $a albinismus circumscriptus $5 e $8 slo 450 $a albinizmus čiastočný $5 e $8 slo 450 $a depigmentácie kože ohraničené $5 e $8 slo 550 $3 sllk_un_auth*d014849 $Y Waardenburg Syndrome $5 B $a Waardenburgov syndróm 550 $3 sllk_un_auth*d014849 $Y Waardenburg Syndrome $5 F $a Waardenburgov syndróm 550 $3 sllk_un_auth*d019009 $Y Proto-Oncogene Proteins c-kit $5 B $a proteíny protoonkogénové c-kit 686 $a C16.320.290.040.600 686 $a C16.320.565.100.102.600 686 $a C16.320.850.080.600 686 $a C17.800.621.440.102.600 686 $a C17.800.827.080.600 686 $a C18.452.648.100.102.600 750 $a Piebaldism $8 eng 801 -0
$a US $b DNLM $c 19920606 801 -2
$a SK $b BA006 $c 20031015 980 $x M
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