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osteogenesis imperfecta
SYS d010013 LBL 00000cz--a2200000o--4500 005 20250606214403.7 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C05.116.099.708.685 065 $a C16.320.737 065 $a C17.300.200.540 066 $a 01 $c 03 150 $a osteogenesis 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 Fragilitas Ossium $2 eng 450 $w v $a Lobstein Disease $2 eng 450 $w v $a Lobsteinova choroba $2 slo 450 $w v $a fragilitas ossium $2 slo 550 $7 sllk_us_auth*d003811 $Y Dentinogenesis Imperfecta $w b $a dentinogenesis imperfecta 550 $7 sllk_us_auth*d003811 $Y Dentinogenesis Imperfecta $w p $a dentinogenesis imperfecta 550 $7 sllk_us_auth*d024042 $Y Collagen Type I $w p $a kolagén typu I 550 $7 sllk_us_auth*d024042 $Y Collagen Type I $w b $a kolagén typu I 680 9-
$i COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I. $2 eng 750 -2
$a Osteogenesis Imperfecta $2 eng 980 $x M
Počet záznamov: 1