Number of the records: 1
neoplázia endokrinná mnohopočetná, typ 2a
SYS d018813 LBL 00000cx--j22000003--45-- 005 20240119201321.2 100 $a 19940523csloy0103----ba0 152 $b mesh 250 $a neoplázia endokrinná mnohopočetná, typ 2a $x BL $x BS $x CF $x CH $x CI $x CL $x CN $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 SC $x SU $x TH $x UL $x UR $x VE $x VI $8 slo 300 1-
$a 95; MEA II, MEN II, & SIPPLE SYNDROME were see NEOPLASMS, MULTIPLE ENDOCRINE 1983-94 $8 eng 300 1-
$a Multiple Endocrine Neoplasia (1966-1994) $8 eng 330 1-
$a A form of multiple endocrine neoplasia characterized by the presence of medullary carcinoma (CARCINOMA, MEDULLARY) of the THYROID GLAND, and usually with the co-occurrence of PHEOCHROMOCYTOMA, producing CALCITONIN and ADRENALINE, respectively. Less frequently, it can occur with hyperplasia or adenoma of the PARATHYROID GLANDS. This disease is due to gain-of-function mutations of the MEN2 gene on CHROMOSOME 10 (Locus: 10q11.2), also known as the RET proto-oncogene that encodes a RECEPTOR PROTEIN-TYROSINE KINASE. It is an autosomal dominant inherited disease. $8 eng 450 $a MEN 2 $5 e $8 eng 450 $a MEN 2a $5 e $8 eng 450 $a Neoplasia, Multiple Endocrine Type 2a $5 e $8 eng 450 $a Neoplasms, Multiple Endocrine Type 2a $5 e $8 eng 450 $a Sipple Syndrome $5 e $8 eng 450 $a MEN2a $5 e $8 slo 450 $a MEN 2 $5 e $8 slo 450 $a MEN 2a $5 e $8 slo 450 $a nádory endokrinné mnohopočetné, typ 2a $5 e $8 slo 450 $a Sippleov syndróm $5 e $8 slo 550 $3 sllk_un_auth*d010673 $Y Pheochromocytoma $5 B $a feochromocytóm 550 $3 sllk_un_auth*d018276 $Y Carcinoma, Medullary $5 B $a karcinóm medulárny 686 $a C04.588.322.400.505 686 $a C04.651.600.505 686 $a C04.700.630.505 686 $a C16.320.700.630.505 686 $a C19.344.400.505 750 $a Multiple Endocrine Neoplasia Type 2a $8 eng 801 -0
$a US $b DNLM $c 19940523 801 -2
$a SK $b BA006 $c 20020709 820 $a coordinate IM with specific endocrine/neoplasm pre-coordinates (IM) + specific histological type (IM) if pertinent $8 eng 980 $x M
Number of the records: 1