Number of the records: 1
Laurenceov-Moonov syndróm
SYS d007849 LBL 00000nx--j22000003--45-- 005 20240119201039.7 100 $a 19990101csloy0103----ba0 152 $b mesh 250 $a Laurenceov-Moonov 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 $8 slo 300 1-
$a 2000 (1966) $8 eng 330 1-
$a An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY. This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity. (From N Engl J Med. 1989 Oct 12;321(15):1002-9) $8 eng 450 $a Laurence-Moon-Biedl Syndrome $5 e $8 eng 450 $a Laurenceov-Moonov-Biedlov syndróm $5 e $8 slo 450 $a degenerácia diencefaloretinálna $5 e $8 slo 550 $3 sllk_un_auth*d008607 $Y Intellectual Disability $5 F $a postihnutie intelektuálne 686 $a C10.228.140.617.500 686 $a C16.131.077.509 750 $a Laurence-Moon Syndrome $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20001114 820 $a note entry term: do not confuse with LAURENCE-MOON-BARDET-BIEDL SYNDROME see BARDET-BIEDL SYNDROME $8 eng 980 $x M
Number of the records: 1