Počet záznamov: 1
Kallmannov syndróm
SYS d017436 LBL 00000nz--a2200000o--4500 005 20250606213430.2 008 920520|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C12.050.351.875.253.096.750 065 $a C12.200.706.316.096.750 065 $a C12.800.316.096.750 065 $a C16.131.939.316.096.750 065 $a C16.320.467 065 $a C19.391.119.096.750 065 $a C19.391.482.600 066 $a 01 $c 03 150 $a Kallmannov syndróm $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 550 $7 sllk_us_auth*d007987 $Y Gonadotropin-Releasing Hormone $w b $a hormón uvoľňujúci gonadotropín 550 $7 sllk_us_auth*d007987 $Y Gonadotropin-Releasing Hormone $w p $a hormón uvoľňujúci gonadotropín 550 $7 sllk_us_auth*d051496 $Y Receptor, Fibroblast Growth Factor, Type 1 $w p $a receptor fibroblastového rastového faktora, typ 1 550 $7 sllk_us_auth*d051496 $Y Receptor, Fibroblast Growth Factor, Type 1 $w b $a receptor fibroblastového rastového faktora, typ 1 665 $a 93 $2 eng 665 $a Hypogonadism (1966-1992) $2 eng 680 9-
$i A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait. $2 eng 750 -2
$a Kallmann Syndrome $2 eng 980 $x M
Počet záznamov: 1