Number of the records: 1
piebaldizmus
SYS d016116 LBL 00000cz--a2200000o--4500 005 20250606214559.1 008 920606|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C16.320.290.040.600 065 $a C16.320.565.100.102.600 065 $a C16.320.850.080.600 065 $a C17.800.621.440.102.600 065 $a C17.800.827.080.600 065 $a C18.452.648.100.102.600 066 $a 01 $c 03 150 $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 $2 slo 450 $w v $a Albinism, Cutaneous $2 eng 450 $w v $a Albinism, Partial $2 eng 450 $w v $a pieboldizmus $2 slo 450 $w v $a albinizmus ohraničený $2 slo 450 $w v $a albinismus circumscriptus $2 slo 450 $w v $a albinizmus čiastočný $2 slo 450 $w v $a depigmentácie kože ohraničené $2 slo 550 $7 sllk_us_auth*d014849 $Y Waardenburg Syndrome $w b $a Waardenburgov syndróm 550 $7 sllk_us_auth*d014849 $Y Waardenburg Syndrome $w p $a Waardenburgov syndróm 550 $7 sllk_us_auth*d019009 $Y Proto-Oncogene Proteins c-kit $w b $a proteíny protoonkogénové c-kit 665 $a 91 $2 eng 665 $a Albinism (1966-1971) $2 eng 665 $a Pigmentation Disorders (1966-1990) $2 eng 680 9-
$i 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. $2 eng 750 -2
$a Piebaldism $2 eng 980 $x M
Number of the records: 1