<HashMap><database>EGA</database><scores/><additional><omics_type>Genomics</omics_type><dataset_type>N/A</dataset_type><full_dataset_link>https://ega-archive.org/datasets/EGAD00010001689</full_dataset_link><sample_count>24</sample_count><description>EGA dataset EGAD00010001689</description><repository>EGA</repository><title>The genotype of LAM disease</title><name_synonyms>CG10236, B130007O04Rik, Lam[[Dm0]], other disease, DmelCG6944, 5430428I19, Dm[[mit]], DmLamin, CT28769, disorders, DmelCG10236, 5]], l(2)25Ec, lam, lamA, AW046674, LamDm[[0]], LamDm[[o]], lamin, TSC, l(2)04643, Dm0, Dm2, Dm(0), Genogroup, Dm1, Dm, diseases, lung lymphangioleiomyomatosis, Diseases, jf27, CG6944, disease or disorder, condition, Dm[[0]], Dm[[o]], diseases and disorders, TSC4, lipoarabinomannan-B, Dm[[2]], misg, alpha3/5, Lam A, human disease, lamin Dm0, DmO, l(2)jf27, LM-A/alpha1, alpha[[3, 74/76, hdln, lamDm[[0]], l(2)gdh-7, PPP1R160, nlam, lamDm0, Lamp, Genotypes, DM[[O]], LAM-B, non-neoplastic, Genogroups, l(2)gdh7, disease, FBgn0002526, D930023J12Rik, Dmo, pulmonary lymphangioleiomyomatosis, Lam Dm[[0]], laminin alpha3/5, LamA, Lam-A, D5, 2459, Lamin Dm[[0]], disorder, lamin Dm[[0]], Homo sapiens disease, medical condition., Lam(Dm0), Lan, Lam, LAM, lanA, Dm[[1]]</name_synonyms><description_synonyms>B130007O04Rik, Lam[[Dm0]], other disease, DmelCG6944, 5430428I19, Neoplasms, DmLamin, CT28769, Benign Neoplasm, Tumor, Malignant, AW046674, LamDm[[0]], Dm(0), diseases, disease or disorder, Dm[[0]], diseases and disorders, TSC4, lipoarabinomannan-B, hereditary., alpha3/5, human disease, lamin Dm0, Biopsies, Malignancy, 74/76, hdln, l(2)gdh-7, nlam, DM[[O]], LAM-B, non-neoplastic, genetic, Neoplasias, FBgn0002526, pulmonary lymphangioleiomyomatosis, laminin alpha3/5, Clients, Lam-A, D5, 2459, Lamin Dm[[0]], disorder, Homo sapiens disease, Malignancies, Lam(Dm0), Lan, Lam, LAM, constitutitional genetic, Dm[[1]], Cancer, Tumors, CG10236, Malignant Neoplasm, Dm[[mit]], disorders, familial, DmelCG10236, 5]], l(2)25Ec, medical condition, lam, lamA, Client, LamDm[[o]], lamin, TSC, l(2)04643, Dm0, Benign, Dm2, Dm1, Dm, lung lymphangioleiomyomatosis, Diseases, Neoplasm, jf27, CG6944, condition, Dm[[o]], Dm[[2]], misg, Lam A, DmO, l(2)jf27, LM-A/alpha1, alpha[[3, lamDm[[0]], Benign Neoplasms, PPP1R160, Cancers, lamDm0, Lamp, Malignant Neoplasms, l(2)gdh7, disease, D930023J12Rik, Dmo, Lam Dm[[0]], Patient, LamA, lamin Dm[[0]], inherited genetic, other neoplasm, lanA, Neoplasia</description_synonyms></additional><is_claimable>false</is_claimable><name>The genotype of LAM disease</name><description>Tumor biopsies from LAM disease were retrospectively analyzed by multiple techniques to characterize the alterations in patients ,to elucidate the landscape of genetic/genomic alterations.</description><dates><updated>2019-09-25 09:51:40</updated></dates><accession>EGAD00010001689</accession><cross_references><TAXONOMY>9606</TAXONOMY><EGA>EGAC00001001148</EGA><EGA>EGAS00001003534</EGA></cross_references></HashMap>