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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **7176 - 7200** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:4195	hyperglycemia	ACACA ACAT1 ACE ACHE ACSM3 AKR1B1 ALDH2 ALDOB ANXA5 APRT ARSA ASAH1 CAT CD33 CD44 CEACAM5 CEL CERS2 CPT1A CPT2 CTSA CYP11A1 CYP1B1 CYP2C9 CYP2E1 DCN DEGS1 DGKD DLD ELOVL1 ELOVL5 ENO1 ENO2 ENPP1 EPHX2 FASN FBXO2 FCGR3B G6PC1 G6PC2 GAD1 GAL3ST1 GALNT2 GCK GFPT1 GFPT2 GGT1 GLDC GLO1 GLUL GPX1 GPX5 GUSB GYS2 HAS2 HK2 HK3 HKDC1 HPGDS HPRT1 HPSE HSD11B1 HSPG2 HTR2A ICAM1 IL1R1 INPP5F KL KLRK1 LDHA LEPR LGALS1 LGALS3 LPCAT3 LPL MBL2 MCAT MGAM MPG NAMPT NEU1 OGG1 PARP1 PC PCK1 PCK2 PDHX PDX1 PFKM PIK3CA PIK3CB PIK3CD PIK3CG PKLR PKM PLA2G2A PLA2G4A PLA2G6 PLAUR PLB1 PNPLA3 PPARGC1A PRKAA2 PRNP PTEN PTGDS PTGS1 PTGS2 RENBP SCD SCP2 SDC1 SDC2 SDC4 SELE SGPL1 SI SIGLEC7 SIRT2 SIRT6 SLC17A5 SLC2A2 SLC2A3 SLC2A4 SLC35A1 SLC35G1 SLC5A1 SMUG1 SOAT1 SORD ST3GAL4 SULT1E1 TKT TM7SF2 UGCG VCAM1 VCAN	10135 10162 1048 10559 1056 10855 10891 1374 1376 142 1462 151056 1545 1559 1571 1583 159371 1634 1636 1738 2023 2026 2053 217 2194 2215 22876 229 22914 22933 231 23583 2538 2571 2590 26232 2645 26503 2673 2678 27036 27306 2731 27349 2739 2752 2876 2880 2990 29956 2998 3037 308 3099 31 3101 3251 3290 3339 3356 3383 353 3554 3651 38 3939 3953 3956 3958 4023 410 4153 427 43 4350 4758 4968 5091 5105 5106 51548 5167 5213 5290 5291 5293 5294 5313 5315 5320 5321 5329 5476 5563 5621 5728 5730 5742 5743 57818 5973 60481 6296 6319 6342 6382 6383 6385 6401 6476 64834 6484 6514 6515 6517 6523 6646 6652 6783 7086 7108 7357 7412 80201 80339 8050 8398 847 8527 8560 8879 8972 9365 945 9514 960 9945	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:11981	morbid obesity Aliases: Severe obesity	ACACB ACE ACHE ACSS2 ATP6AP2 BAAT CNTN3 CPT1B CYP2E1 ENPP1 FDFT1 GAD2 GGT1 GHRL GPX1 LPIN1 LPL MRC1 NAMPT NCAN PFKFB3 PNPLA3 SCD SLC2A4 TKTL1	10135 10159 1375 1463 1571 1636 2222 23175 2572 2678 2876 32 4023 43 4360 5067 5167 51738 5209 55902 570 6319 6517 80339 8277	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:4676	uremia Aliases: UREMIA OF renal ORIGIN	ACE ACSS2 AGL AGXT AKR1B1 ALPL ALPP APRT ATP6AP2 ATRNL1 CAT COMT CTSA CYP11B2 CYP24A1 CYP3A4 DCN DEGS1 DGKE ENPP1 FCGR3B G6PC1 GCNT2 GGT1 GLA HAGH HSPG2 ICAM1 IDH2 KL KLB LCAT LYZ MASP1 MBL2 NAMPT OCRL PARP1 PIK3C3 PKD1 PKD2 PLA2G15 PLA2G7 PTGS1 PTGS2 RENBP RGN SDC1 SDC2 SELL SLC17A5 SLC35G1 SMUG1 TM7SF2 UMOD VCAM1	10135 10159 1312 142 152831 1576 1585 1591 159371 1634 1636 178 189 2215 231 23583 23659 249 250 2538 26033 26503 2651 2678 2717 3029 3339 3383 3418 353 3931 4069 4153 4952 5167 5289 5310 5311 5476 55902 5648 5742 5743 5973 6382 6383 6402 7108 7369 7412 7941 847 8526 8560 9104 9365	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0110425	dilated cardiomyopathy 1A Aliases: CDCD1 dilated cardiomyopathy with conduction defect 1 familial dilated cardiomyopathy with conduction defect due to LMNA mutation	ABO ACACA ACE ALDH7A1 ATP6AP2 BDH1 CAT CHI3L1 CPT1A CPT2 CYP11B2 CYP19A1 CYP1A2 CYP2E1 DAG1 DBT DOLK ECI1 ENO1 FASN FKRP FKTN FUT3 GBE1 GPX1 GPX3 HPRT1 HSD17B2 IDH1 IL18R1 IL1RL1 KL LGALS3 LY75 MBL2 MDH1 MGAM MGAT1 MMUT MPI MRC1 NAMPT NCAM1 PCCA PCCB PGM1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G7 PLB1 PNPLA2 PRG2 PRKAA2 PTEN PTGS2 RENBP SCD SDC1 SDC4 SDHA SDHB SLC2A4 SLC35B2 SLC5A1 SMUG1 SRGN ST3GAL4 SULF2 SULT1E1 TM7SF2 UGT8 VTCN1	10135 10159 1116 1374 1376 151056 1544 1571 1585 1588 1605 1629 1632 1636 2023 2194 2218 22845 23583 2525 2632 28 2876 2878 31 3251 3294 3417 347734 3958 4065 4153 4190 4245 4351 4360 4594 4684 501 5095 5096 5236 5290 5291 5293 5294 5552 5553 5563 55959 57104 5728 5743 5973 622 6319 6382 6385 6389 6390 6484 6517 6523 6783 7108 7368 79147 7941 79679 847 8809 8972 9173 9365	Homo sapiens (human)	DisGeNET
DOID:3008	invasive ductal carcinoma Aliases: Infiltrating ductal carcinoma of breast Invasive ductal carcinoma, NST ductal adenocarcinoma	ABO ADH4 AKT1 ALDOA ASAH1 ATP6AP2 CD14 CD44 CHI3L1 CTSA CYP19A1 DCN DHCR24 DHRS11 DPEP1 ENO1 FUT3 GAL3ST1 GPX3 HMMR HPGDS HPSE HSD17B12 HSD17B1 HSD17B7 IDH1 KL KLB LGALS1 LGALS3 MCAT MGAT5 MGLL NAMPT NEU1 PCNA PDIA3 PFKFB4 PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1C PLCB2 POFUT1 PRKAA2 PSMD10 PTEN PTGS2 RGN SDC1 SELE SLC35B2 SMUG1 ST8SIA1 SULF2 UGCG VTCN1	10135 10159 10855 1116 11343 127 152831 1588 1634 1718 1800 2023 207 226 23396 23509 23583 2525 27306 27349 28 2878 2923 3161 3292 3417 347734 3956 3958 4249 427 4758 5111 51144 51478 5210 5290 5291 5293 5294 5330 5476 5563 55959 5716 5728 5743 6382 6401 6489 7357 79154 79679 9104 929 9365 9514 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:7997	thyrotoxicosis	ABO ACACA ACE ALG1 ANXA5 APRT ATP6AP2 B3GNT2 BAAT BDH1 CALR CAT CD14 CMAS COMT CS CYP19A1 CYP1A1 CYP21A2 CYP27B1 CYP2C9 CYP2R1 CYP7A1 DEGS1 ENPP2 FCER2 FCGR3B FUT2 GAD1 GAD2 GLO1 GLUL GPX1 ICAM1 IL18R1 IL18RAP IL1RL1 KLRC1 LGALS9 LYZ MBL2 NAMPT NCAM1 NT5E OGG1 PARP1 PC PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PLA2G1B PLA2G2A PLA2G6 PPT1 PRKAA2 PTEN PTGDS SCD SELE SELL SIGLEC1 SLC2A3 SLC2A4 SMUG1 ST3GAL1 ST6GAL1 TM7SF2 UGDH UGT1A1 UGT2B17 VCAM1	10135 10159 10678 120227 1312 142 1431 1543 1559 1581 1588 1589 1594 1636 2208 2215 23583 2524 2571 2572 2739 2752 28 2876 308 31 3383 353 3821 3965 4069 4153 4684 4907 4968 5091 5130 5168 5290 5291 5293 5294 5319 5320 54658 5538 5563 55907 56052 570 5728 5730 622 6319 6401 6402 6480 6482 6515 6517 6614 7108 7358 7367 7412 811 8398 847 8560 8807 8809 9173 929	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:12361	Graves' disease Aliases: Grave's disease Graves disease exophthalmic goiter	ABO ACACA ACE ADIPOQ ALG1 ANXA5 APRT ATP6AP2 B3GNT2 BAAT BDH1 CALR CAT CD14 CMAS COMT CS CYP19A1 CYP1A1 CYP21A2 CYP27B1 CYP2C9 CYP2R1 CYP7A1 DEGS1 ENPP2 FCER2 FCGR3B FUT2 GAD1 GAD2 GLO1 GLUL GPX1 ICAM1 IL18R1 IL18RAP IL1RL1 KLRC1 LGALS9 LYZ MBL2 NAMPT NCAM1 NT5E OGG1 PARP1 PC PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PLA2G1B PLA2G2A PLA2G6 PPT1 PRKAA2 PTEN PTGDS SCD SELE SELL SIGLEC1 SLC2A3 SLC2A4 SMUG1 ST3GAL1 ST6GAL1 TM7SF2 TNF TP53 UGDH UGT1A1 UGT2B17 VCAM1	10135 10159 10678 120227 1312 142 1431 1543 1559 1581 1588 1589 1594 1636 2208 2215 23583 2524 2571 2572 2739 2752 28 2876 308 31 3383 353 3821 3965 4069 4153 4684 4907 4968 5091 5130 5168 5290 5291 5293 5294 5319 5320 54658 5538 5563 55907 56052 570 5728 5730 622 6319 6401 6402 6480 6482 6515 6517 6614 7108 7124 7157 7358 7367 7412 811 8398 847 8560 8807 8809 9173 929 9370	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:7998	hyperthyroidism Aliases: overactive thyroid	ABO ACACA ACE ADIPOQ ALG1 ANXA5 APRT ATP6AP2 B3GNT2 BAAT BDH1 CALR CAT CD14 CMAS COMT CS CYP19A1 CYP1A1 CYP21A2 CYP27B1 CYP2C9 CYP2R1 CYP7A1 DEGS1 ENPP2 FCER2 FCGR3B FUT2 GAD1 GAD2 GLO1 GLUL GPX1 ICAM1 IL18R1 IL18RAP IL1RL1 KLRC1 LGALS9 LYZ MBL2 NAMPT NCAM1 NR1D1 NT5E OGG1 PARP1 PC PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PLA2G1B PLA2G2A PLA2G6 PPARGC1A PPT1 PRKAA2 PTEN PTGDS SCD SELE SELL SIGLEC1 SLC2A3 SLC2A4 SMUG1 ST3GAL1 ST6GAL1 TM7SF2 UGDH UGT1A1 UGT2B17 VCAM1	10135 10159 10678 10891 120227 1312 142 1431 1543 1559 1581 1588 1589 1594 1636 2208 2215 23583 2524 2571 2572 2739 2752 28 2876 308 31 3383 353 3821 3965 4069 4153 4684 4907 4968 5091 5130 5168 5290 5291 5293 5294 5319 5320 54658 5538 5563 55907 56052 570 5728 5730 622 6319 6401 6402 6480 6482 6515 6517 6614 7108 7358 7367 7412 811 8398 847 8560 8807 8809 9173 929 9370 9572	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:6000	congestive heart failure Aliases: CHF Cardiac Failure Congestive Congestive heart disease Weak heart	ABO ACACA ACADM ACADS ACAN ACAT1 ACE ACHE ACLY ACOT7 ACSL5 ACSL6 ACSS2 ADIPOQ ADRB3 AGPAT2 AKR1B1 ALDH2 ALDH7A1 ALG12 ALG9 ALOX12 ALOX15 AMACR ANXA5 APRT ARSB ARSD ATP6AP2 ATP6V1A BDH1 CALR CAT CBR3 CD14 CD44 CDS1 CDS2 CERS1 CERS5 CHGA CHI3L1 CHPT1 CNTN5 COG7 CPT1A CPT1B CPT2 CS CYP11B1 CYP11B2 CYP1A1 CYP1A2 CYP1B1 CYP27B1 CYP2B6 CYP2C19 CYP2E1 CYP2J2 CYP3A4 CYP3A5 CYP4F3 DAG1 DCN DGAT1 DLD DLST EBP ELOVL6 ENO2 ENPP1 EPHX2 FADS1 FADS2 FASN FDPS FH FKRP FKTN FMOD G6PD GAD1 GAL3ST1 GALNT1 GAPDH GBA1 GBE1 GLA GLB1 GNPTAB GPD1L GUSB HADH HADHA HADHB HJV HK2 HMGCL HPGDS HSD11B1 HSPG2 HTR2A ICAM1 IDS IGF2R IL1RL1 INPPL1 ISYNA1 ITPK1 KL KLRK1 LCAT LEPR LGALS16 LGALS1 LGALS3 LIPC LPIN2 LPL LY75 LYZ MCAT MDH2 ME1 MGAT1 MMUT MPI MRC1 NAGLU NAMPT NANS NCAM1 NDUFAB1 NPL NT5E NTM OGA OGDH OGT OLR1 PAFAH1B1 PARP1 PCK1 PGK1 PIGF PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PKD2 PLA2G15 PLA2G2A PLA2G7 PLCD1 PLCE1 PLCG1 PLD1 PLD2 PLPP3 PNPLA2 POFUT1 PPP1CC PPP1R3A PPT1 PRKAA2 PTEN PTGIS PTGS1 PTGS2 RBP4 RENBP SCD SDC1 SDC2 SDC4 SDCBP2 SDHA SDHB SDHC SDHD SELE SELP SFTPD SGPL1 SIRT6 SLC17A5 SLC26A2 SLC2A10 SLC2A4 SLC33A1 SLC35A1 SLC39A8 SLC5A1 SMPD1 SMPD2 SMUG1 SOAT1 SPHK1 SRGN STS SUCLA2 SULT1E1 TM7SF2 TMTC3 TNF TPI1 UCP2 UGT1A1 UGT2B7 UMOD VCAM1 XYLT1 XYLT2	10135 10159 1040 10555 10559 10682 10715 10724 1113 1116 11332 1374 1375 1376 142 1431 148003 148738 1543 1544 1545 155 1555 1557 1571 1573 1576 1577 1584 1585 1594 160418 1605 1634 1636 1738 1743 176 1836 2026 2053 217 2194 2218 2224 2271 22914 231 23171 23305 2331 23509 23583 23600 23659 239 246 2539 2571 2589 2597 2629 2632 26503 27111 2717 2720 27306 27349 28 2990 3030 3032 3033 308 3099 31 3155 3290 3339 3356 3383 34 3423 3482 35 353 3636 3705 38 3931 3953 3956 3958 3990 3992 4023 4051 4065 4069 411 412 414 4191 4199 4245 43 4351 4360 4594 4669 4684 47 4706 4907 4967 4973 501 5048 50863 5105 51196 51477 51548 5167 51703 523 5230 5281 5290 5291 5293 5294 5310 5311 5320 5333 5335 5337 5338 53942 54187 54658 5501 5506 5538 5552 5563 55902 56994 57104 5728 5740 5742 5743 5950 5973 622 6319 6382 6383 6385 6389 6390 6391 6392 6401 6403 64116 64131 64132 6441 6517 6523 6609 6610 6646 6783 7108 7124 7167 7351 7364 7369 7412 79071 79087 79147 79158 7941 79796 80896 81031 811 847 8473 8613 8694 874 8760 8803 8877 8879 91012 9173 91949 9197 929 9365 9370 9415 9514 960 9663	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:1289	neurodegenerative disease Aliases: degenerative disease	ACADM ACE ACHE ACO2 ACOX1 ACSBG1 ADPRS AGPAT3 AKR1A1 ALDH2 ALOX12 ALOX5 ALPP ARSA ASAH1 ATP6AP2 ATRNL1 B3GAT1 CAT CCDC115 CD14 CD33 CD38 CHAT CHGA CHI3L1 CHIT1 CLEC10A CLEC16A CLN5 CNTN2 COLEC11 COMT CYP19A1 CYP27A1 CYP2B6 CYP2U1 CYP46A1 CYP7B1 DAG1 DEGS1 DEGS2 DHCR24 DLST ELOVL4 ENO2 EPM2A FCN2 FDPS FIG4 FOLR2 G6PD GAA GAD1 GALC GAPDH GBA1 GDPD5 GLB1 GLO1 GLUL GM2A GPNMB GPX3 GUSB HEXA HEXB HIBCH HK1 HK2 HPGDS HPSE ICAM1 IDH2 INPPL1 KL L2HGDH LGALS3 LIPC LPL MANEAL MGLL MRC1 MTM1 MTMR2 MUTYH MYORG NAGLU NAGPA NAMPT NDUFAB1 OARD1 OGA OGDH OGG1 OGT PARP10 PARP1 PDIA3 PGP PIK3CA PIK3CB PIK3CD PIK3CG PKD2 PLA2G1B PLA2G2A PLA2G4A PLA2G5 PLA2G6 PLB1 PLCG2 PNP PNPLA6 PNPLA7 PPT1 PRKAA2 PRKAG2 PRKAG3 PRNP PTEN PTGES3 PTGES PTGS2 QPRT RENBP RPE SARM1 SCP2 SDHA SFTPA1 SGPL1 SGSH SI SIGLEC7 SIRT2 SIRT6 SLC17A5 SLC33A1 SMUG1 SPHK2 SPTLC1 SPTLC3 STS SUCLA2 SYNJ1 TIGAR TKT TMED9 TPI1 UNG VCAN	10135 10159 10327 10457 10462 10558 10724 10728 10855 10858 10908 1103 1113 1116 1118 11343 113612 1203 123099 1312 142 1462 149175 151056 1555 1588 1593 1605 1636 1718 1743 2026 217 221443 2220 2224 22933 23098 23205 23274 23475 2350 23583 239 240 250 2539 2548 2571 2581 2597 26033 26275 2629 26503 27036 27087 2720 27306 2739 2752 2760 283871 2878 2923 2990 3073 3074 3098 3099 3383 34 3418 3636 375775 3958 3990 4023 410 412 427 43 4360 4534 4595 4669 4706 4860 4967 4968 50 51 51172 51422 51548 5290 5291 5293 5294 5311 5319 5320 5321 5322 5336 53632 54732 54936 55304 5538 5563 5621 56848 56894 57103 5728 5743 57462 5973 6120 6342 6389 6448 6476 653509 6785 6900 7086 7167 7374 78989 7957 79944 81544 8398 84317 847 8473 84875 8560 8803 8867 8879 8898 9197 929 9365 9420 945 952 9536 9896	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:1074	kidney failure Aliases: renal failure	A4GALT ACE ACSL4 ACSS2 AGL AGPAT2 AGXT AKR1B1 ALOX12B ALOX5 ALPP APRT ARSA ATP6AP2 ATRNL1 CAT CHGA COG1 CPM CPT2 CTNS CTSA CYP11B2 CYP1A2 CYP24A1 CYP2C19 CYP2C9 CYP3A4 CYP3A5 CYP4F3 DCN DEGS1 DGKE DHDDS EBP ENPP1 FCGR3B G6PC1 GCNT2 GGT1 GLA GRHPR HAGH HPRT1 HPSE2 HPSE HSD11B2 HSPG2 ICAM1 IDH2 INPP5E KL KLB LCAT LDHA LGALS3 LYZ MASP1 MBL2 ME1 MMUT MSLN NAGLU NAMPT NCAN OCRL OGA OLR1 PARP1 PGAM2 PGK1 PIK3C3 PKD1 PKD2 PLA2G15 PLA2G7 PNPLA3 PNPLA6 PPARGC1A PRKAA2 PRPS1 PTGS1 PTGS2 PYGM RENBP RGN SDC1 SDC2 SELE SELL SELP SLC17A5 SLC2A2 SLC35G1 SLC37A4 SLC3A1 SLC5A1 SMC3 SMUG1 STS SULT2B1 TLR2 TLR4 TM7SF2 TMEM260 UGT2B17 UMOD VCAM1 VCAN XYLT1 XYLT2	10135 10159 10232 10555 10682 10724 10855 10891 10908 1113 1368 1376 142 1462 1463 1497 152831 1544 1557 1559 1576 1577 1585 1591 159371 1634 1636 178 189 2182 2215 231 23583 23659 240 242 250 2538 2542 26033 26503 2651 2678 2717 3029 3251 3291 3339 3383 3418 353 3931 3939 3958 4051 4069 410 412 4153 4199 4594 4669 4952 4973 5167 5224 5230 5289 5310 5311 53947 5476 54916 5563 55902 5631 5648 56623 5742 5743 5837 5973 60495 6382 6383 6401 6402 6403 64131 64132 6514 6519 6523 6820 7097 7099 7108 7367 7369 7412 7941 79947 80339 847 8526 8560 9104 9126 9365 9380 9382	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:3498	pancreatic ductal adenocarcinoma Aliases: ductal adenocarcinoma of the pancreas	ABO ACACB ACE AKR1B10 AKR7A2 APRT ARSA ATP6AP2 B3GALNT1 CALR CD44 CEACAM5 CEACAM6 CEL CEMIP CHGA CHKA CHST15 COL9A2 CYP1B1 CYP3A5 CYP4F2 CYP4F3 DAG1 DPEP1 ENO1 FASN FBP1 FCN2 FOLR1 FOLR2 FUT8 GALNT5 GOLPH3 GOT1 GPC1 GPC5 HK1 IDH1 IDUA L1CAM LGALS1 LGALS3 LGALS4 MDH1 MMUT MRC1 MSLN MUTYH NAMPT NEU2 NT5E PAFAH1B2 PARP1 PDHX PGAM1 PGK1 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLD1 PNPLA2 PRKAA2 PRNP PTEN PTGS2 RECK REG3G SIGLEC7 SIRT6 SMUG1 SOAT1 ST6GAL1 VCAM1 VNN1	10135 10159 10232 1048 1056 1113 1119 11227 1298 130120 142 1545 1577 1605 1636 1800 2023 2194 2203 2220 2262 2348 2350 23583 2530 27036 28 2805 2817 3098 32 3417 3425 353 3897 3956 3958 3960 4051 410 4190 4360 4594 4595 4680 4759 4907 5049 51363 51548 5223 5230 5290 5291 5293 5294 5315 5337 5563 5621 57016 57104 57214 5728 5743 64083 6480 6646 7412 8050 811 8434 8529 8574 8706 8876 960	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:6587	breast tubular carcinoma Aliases: Invasive tubular carcinoma of breast invasive tubular breast carcinoma tubular carcinoma of breast	CDH13	1012	Homo sapiens (human)	DisGeNET
DOID:4916	pituitary carcinoma Aliases: carcinoma of the Pituitary gland	CD44 CDH13 HSD11B2 IDH1 IDH2 LDHA PIK3CA PIK3CB PIK3CD PIK3CG PRKAA2 PTEN PTGS2 SCP2 SMUG1 STS TBXAS1	1012 23583 3291 3417 3418 3939 412 5290 5291 5293 5294 5563 5728 5743 6342 6916 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:1785	pituitary cancer Aliases: Pituitary gland neoplasm malignant Pituitary neoplasm malignant tumor of pituitary gland neoplasm of pituitary gland pituitary gland cancer pituitary neoplasm	CD44 CDH13 HSD11B2 IDH1 IDH2 LDHA PIK3CA PIK3CB PIK3CD PIK3CG PRKAA2 PTEN PTGS2 SCP2 SMUG1 STS TBXAS1	1012 23583 3291 3417 3418 3939 412 5290 5291 5293 5294 5563 5728 5743 6342 6916 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:461	muscle benign neoplasm Aliases: Myomatous neoplasm Myomatous tumor muscle neoplasm muscle tissue neoplasm neoplasm of muscle	CDH13 FH	1012 2271	Homo sapiens (human)	DisGeNET
DOID:4045	muscle cancer Aliases: malignant neoplasm of muscle malignant tumor of muscle malignant tumor of the Muscle myosarcoma	CDH13 FH	1012 2271	Homo sapiens (human)	DisGeNET
DOID:4247	coronary restenosis	ACE CDH13 MBL2 TNF TP53	1012 1636 4153 7124 7157	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:3151	skin squamous cell carcinoma Aliases: Epidermoid skin carcinoma	AKR1C3 APRT CD44 CD55 CDH13 CYP21A2 FUT1 GLB1 HPGDS HSD11B2 INPP5A MMUT NCAM1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGDS PTGS2 SDC1 SDC2 SIRT6 SMUG1 SOAT1 SPHK2 ST3GAL1 STT3A	1012 1589 1604 23583 2523 2720 27306 3291 353 3632 3703 4594 4684 51548 5290 5291 5293 5294 56848 5728 5730 5743 6382 6383 6482 6646 8644 960	Homo sapiens (human)	DisGeNET
DOID:2999	granulosa cell tumor Aliases: Granulosa cell neoplasm Granulosa cell tumor, adult type Granulosa cell tumour, sarcomatoid malignant granulosa cell neoplasm	CDH13 CYP17A1 CYP19A1 PKM PTEN PTGS2 TKTL1	1012 1586 1588 5315 5728 5743 8277	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0050789	tarsal-carpal coalition syndrome	ABO ALOX5 CD44 CDH13 CYB5R3 GAPDH GLB1 HPGDS MRC1 NEU1 PLAUR PRSS8 PTEN PTGS2 TM7SF2 TNKS UPP2	1012 151531 1727 240 2597 2720 27306 28 4360 4758 5329 5652 5728 5743 7108 8658 960	Homo sapiens (human)	DisGeNET
DOID:11120	psychologic dyspareunia Aliases: Dyspareunia, psychogenic Non-organic dyspareunia	ACE ACHE ACSS2 ALDH7A1 CDH13 CYP19A1 ENO2 HEXB HJV HMGCS2 HS6ST1 LPL PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PLA2G15 PNPLA2 SDC1 SOAT1	1012 148738 1588 1636 2026 23659 3074 3158 4023 43 501 5130 5290 5291 5293 5294 55902 57104 6382 6646 9394	Homo sapiens (human)	DisGeNET
DOID:1875	impotence Aliases: Sexual impotence erectile dysfunction	ACE ACHE ACSS2 AKT1 ALDH7A1 BAD CDH13 CYP19A1 ENO2 HEXB HJV HMGCS2 HS6ST1 LPL PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PLA2G15 PNPLA2 SDC1 SOAT1 TNF	1012 148738 1588 1636 2026 207 23659 3074 3158 4023 43 501 5130 5290 5291 5293 5294 55902 57104 572 6382 6646 7124 9394	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0060548	luminal breast carcinoma A Aliases: Luminal A Breast Carcinoma	ACACA CDH13 CYP19A1 CYP7B1 FASN GLCE H6PD HMMR IDH2 IL18R1 PARP1 PDHB PGLS PIK3CA PLCG1 PTEN SMUG1	1012 142 1588 2194 23583 25796 26035 31 3161 3418 5162 5290 5335 5728 8809 9420 9563	Homo sapiens (human)	DisGeNET DisGeNET
DOID:670	amphetamine abuse	ACHE ACSL6 CD55 CDH13 COMT GAD1 GAD2 HS3ST4 LARGE1 NPY1R	1012 1312 1604 23305 2571 2572 43 4886 9215 9951	Homo sapiens (human)	DisGeNET Alliance of Genome Resources

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