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Urbachova-Wiethova lipoidproteinóza
SYS d008065 LBL 00000cz--a2200000o--4500 005 20250606214602.3 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 065 $a C08.618.490.500 065 $a C16.320.850.595 066 $a 01 $c 03 150 $a Urbachova-Wiethova lipoidproteinóza $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 Lipoproteinosis $2 eng 450 $w v $a Urbach-Wiethe Disease $2 eng 450 $w v $a proteinóza lipidová $2 slo 450 $w v $a lipoproteinóza $2 slo 450 $w v $a Urbachova-Wiethova choroba $2 slo 550 $7 sllk_us_auth*d057770 $Y Hyaline Fibromatosis Syndrome $w p $a syndróm hyalínovej fibromatózy 550 $7 sllk_us_auth*d008074 $Y Lipoproteins $w b $a lipoproteíny 550 $7 sllk_us_auth*d057770 $Y Hyaline Fibromatosis Syndrome $w b $a syndróm hyalínovej fibromatózy 665 $a 2007 (1975) $2 eng 680 9-
$i An autosomal recessive disorder characterized by glassy degenerative thickening (hyalinosis) of SKIN; MUCOSA; and certain VISCERA. This disorder is caused by mutation in the extracellular matrix protein 1 gene (ECM1). Clinical features include hoarseness and skin eruption due to widespread deposition of HYALIN. $2 eng 750 -2
$a Lipoid Proteinosis of Urbach and Wiethe $2 eng 980 $x M
Number of the records: 1