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Papillonova-Lefevreova choroba
SYS d010214 LBL 00000nx--j22000003--45-- 005 20240119201120.4 100 $a 19990101csloy0103----ba0 152 $b mesh 250 $a Papillonova-Lefevreova choroba $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 91(75); was see under KERATOSIS PALMARIS ET PLANTARIS 1975-90 (which became KERATODERMA, PALMOPLANTAR 1993) $8 eng 330 1-
$a Rare, autosomal recessive disorder occurring between the first and fifth years of life. It is characterized by palmoplantar keratoderma with periodontitis followed by the premature shedding of both deciduous and permanent teeth. Mutations in the gene for CATHEPSIN C have been associated with this disease. $8 eng 550 $3 sllk_un_auth*d020789 $Y Cathepsin C $5 F $a katepsín C 686 $a C16.320.850.475.600 686 $a C17.800.428.435.600 686 $a C17.800.827.475.600 750 $a Papillon-Lefevre Disease $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20070706 980 $x M
Počet záznamov: 1