Number of the records: 1
dentinogenesis imperfecta
SYS d003811 LBL 00000nx--j22000003--45-- 005 20240119201116.7 100 $a 19990101csloy0103----ba0 152 $b mesh 250 $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 $8 slo 300 1-
$a 65 $8 eng 330 1-
$a 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. $8 eng 450 $a Hereditary Opalescent Dentin $5 e $8 eng 450 $a dentinogenesis imperfecta hereditaria $5 e $8 slo 550 $3 sllk_un_auth*d010013 $Y Osteogenesis Imperfecta $5 F $a osteogenesis imperfecta 550 $3 sllk_un_auth*d010013 $Y Osteogenesis Imperfecta $5 B $a osteogenesis imperfecta 686 $a C07.650.800.270 686 $a C07.793.700.270 686 $a C16.131.850.800.270 750 $a Dentinogenesis Imperfecta $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20000330 980 $x M
Number of the records: 1