Počet záznamov: 1
dentinogenesis imperfecta
SYS d003811 LBL 00000nz--a2200000o--4500 005 20260512091048.8 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C07.650.800.270 065 $a C07.793.700.270 065 $a C16.131.850.800.270 066 $a 01 $c 03 150 $a dentinogenesis imperfecta $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 Hereditary Opalescent Dentin $2 eng 450 $w v $a dentinogenesis imperfecta hereditaria $2 slo 550 $7 sllk_us_auth*d010013 $Y Osteogenesis Imperfecta $w p $a osteogenesis imperfecta 550 $7 sllk_us_auth*d010013 $Y Osteogenesis Imperfecta $w b $a osteogenesis imperfecta 665 $a 65 $2 eng 680 9-
$i An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops poorly with low mineral content while the pulp canal is obliterated. $2 eng 750 -2
$a Dentinogenesis Imperfecta $2 eng 980 $x M
Počet záznamov: 1