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hypoplázia kože, fokálna
SYS d005489 LBL 00000cz--a2200000n--4500 005 20250606215916.1 008 920405|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 $d BA006 065 $a C05.116.099.370.380 065 $a C16.131.077.350.424 065 $a C16.131.831.350.424 065 $a C16.320.322.186 065 $a C16.320.850.250.424 065 $a C17.800.804.350.424 065 $a C17.800.827.250.424 066 $a 01 $c 03 150 $a hypoplázia kože, fokálna $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 Dermal Hypoplasia, Focal $2 eng 450 $w v $a Goltz Gorlin Syndrome $2 eng 450 $w v $a Goltz Syndrome $2 eng 450 $w v $a hypoplázia kože, ložisková $2 slo 450 $w v $a Goltzov syndróm $2 slo 450 $w v $a Goltzov-Gorlinov syndróm $2 slo 665 $a 91(85); was see under ECTODERMAL DYSPLASIA 1987-90, was see under ECTODERMAL DEFECT, CONGENITAL 1985-86; GOLTZ-GORLIN SYNDROME was see FOCAL DERMAL HYPOPLASIA 1985-92 $2 eng 665 $a Abnormalities, Multiple (1968-1984) $2 eng 665 $a Skin (1966-1984) $2 eng 665 $a Skin Diseases (1966-1984) $2 eng 680 9-
$i A genetic skin disease characterized by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an X-linked dominant trait. $2 eng 680 $a do not confuse entry term GOLTZ-GORLIN SYNDROME with GORLIN-GOLTZ SYNDROME see BASAL CELL NEVUS SYNDROME $2 eng 750 -2
$a Focal Dermal Hypoplasia $2 eng 980 $x M
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