Number of the records: 1  

syndróm bazocelulárneho névu

  1. SYSd001478
    LBL
      
    00000cz--a2200000n--4500
    005
      
    20250606213806.7
    008
      
    920425|||anznnbabn-----------|-a|a------
    040
      
    $b slo $a DNLM $d BA006 $d BA006
    065
      
    $a C04.182.089.530.690.150
    065
      
    $a C04.557.470.200.165.150
    065
      
    $a C04.557.470.565.165.150
    065
      
    $a C04.700.175
    065
      
    $a C05.116.099.105
    065
      
    $a C05.500.470.690.150
    065
      
    $a C07.320.450.670.130
    065
      
    $a C16.131.077.130
    065
      
    $a C16.320.700.175
    066
      
    $a 01 $c 03
    150
      
    $a syndróm bazocelulárneho névu $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 Gorlin Syndrome $2 eng
    450
      
    $w v $a Nevoid Basal Cell Carcinoma Syndrome $2 eng
    450
      
    $w v $a Nevus Syndrome, Basal Cell $2 eng
    450
      
    $w v $a Gorlinov syndróm $2 slo
    450
      
    $w v $a Gorlinov-Goltzov syndróm $2 slo
    450
      
    $w v $a syndróm karcinómu bazálnych buniek névoidných $2 slo
    450
      
    $w v $a syndroma basal-cell nevus $2 slo
    450
      
    $w v $a NBCCS $2 slo
    450
      
    $w v $a syndróm névoidného bazocelulárneho karcinómu $2 slo
    665
      
    $a 91(80); was see under CARCINOMA, BASAL CELL 1980-90 $2 eng
    665
      
    $a Bone Cyst (1966-1979) $2 eng
    665
      
    $a Carcinoma, Basal Cell (1966-1979) $2 eng
    665
      
    $a Jaw Diseases (1967-1979) $2 eng
    665
      
    $a Jaw Neoplasms (1967-1979) $2 eng
    665
      
    $a Skin Neoplasms (1967-1979) $2 eng
    665
      
    $a specific jaw disease (1967-1979) $2 eng
    665
      
    $a specific jaw neoplasm (1967-1979) $2 eng
    665
      
    $a Syndrome (1972-1979) $2 eng
    680
    9-
    $i Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant. $2 eng
    680
      
    $a coordinate IM with precoordinated organ/neoplasm (IM or NIM) only if pertinent; do not confuse entry term GORLIN-GOLTZ SYNDROME with GOLTZ- GORLIN SYNDROME see FOCAL DERMAL HYPOPLASIA $2 eng
    750
    -2
    $a Basal Cell Nevus Syndrome $2 eng
    980
      
    $x M
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.