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Camuratiho-Engelmannov syndróm
SYS d003966 LBL 00000cx--j22000003--45-- 005 20240119195606.5 100 $a 19921111csloy0103----ba0 152 $b mesh 250 $a Camuratiho-Engelmannov 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 2007(1975) $8 eng 330 1-
$a An autosomal dominant form of dysplasia that is characterized by progressive thickening of diaphyseal cortex of long bones. Mutations in the gene that encodes TRANSFORMING GROWTH FACTOR BETA1 are one cause of this disorder. $8 eng 450 $a Diaphyseal Dysplasia, Progressive $5 e $8 eng 450 $a Engelmann's Disease $5 e $8 eng 450 $a dysplázia diafýzová progresívna $5 e $8 slo 450 $a Engelmannova choroba $5 e $8 slo 450 $a dysplasia progressiva diaphysaria $5 e $8 slo 450 $a osteopathia hyperostotica multiplex infantilis $5 e $8 slo 686 $a C05.116.099.708.180 686 $a C16.320.144 750 $a Camurati-Engelmann Syndrome $8 eng 801 -0
$a US $b DNLM $c 19921111 801 -2
$a SK $b BA006 $c 20070201 980 $x M
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