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*155120 - A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 11; ADAM11
Gene summaries Genetic tests Medical literature
*602957 - CHEMOKINE, CC MOTIF, LIGAND 22; CCL22
Cytogenetic locations: 20525891
*603710 - A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 23; ADAM23
Cytogenetic locations: 19693107
*619495 - ADAM METALLOPEPTIDASE DOMAIN-CONTAINING PROTEIN 18; ADAM18
Cytogenetic locations: 12200459
*603709 - A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 22; ADAM22
Cytogenetic locations: contiguous
#613205 - MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED
*607003 - THYMIC STROMAL LYMPHOPOIETIN; TSLP
Cytogenetic locations: 24094650
*150330 - LAMIN A/C; LMNA
LAMIN A, INCLUDED
Cytogenetic locations: 18348272
*606188 - A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 28; ADAM28
Cytogenetic locations: -
*601520 - CHEMOKINE, CC MOTIF, LIGAND 17; CCL17
Cytogenetic locations: 602354
*605548 - A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 15; ADAM15
Cytogenetic locations: 118507
156000 - MENIERE DISEASE
#610489 - PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1; PPNAD1
Cytogenetic locations: 12828408
%164220 - SCHILBACH-ROTT SYNDROME; SBRS
*604487 - OTOGELIN; OTOG
Cytogenetic locations: 10655058
#601552 - TRABOULSI SYNDROME
Cytogenetic locations: 28749053
*602713 - A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 9; ADAM9
Cytogenetic locations: LOXL2
*601880 - CHEMOKINE, CX3C MOTIF, LIGAND 1; CX3CL1
Cytogenetic locations: 11477410
*600582 - ASPARTATE BETA-HYDROXYLASE; ASPH
JUNCTIN, INCLUDED
Cytogenetic locations: 10767180
#601214 - NAXOS DISEASE; NXD
Cytogenetic locations: 19067702
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