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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 **4426 - 4450** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:4784	immune-complex glomerulonephritis Aliases: Immune Complex Glomerulonephritis	LGALS9	3965	Homo sapiens (human)	DisGeNET
DOID:4022	ureterocele	PIGP PIGQ	51227 9091	Homo sapiens (human)	DisGeNET
DOID:3076	adult astrocytic tumor Aliases: adult astrocytic tumour adult astrocytoma	CHST15 ENPP1 IDH1 IDH2 LGALS3	3417 3418 3958 51363 5167	Homo sapiens (human)	DisGeNET
DOID:700	mitochondrial metabolism disease	ACACA ACOX1 AGK ALDH2 APRT ARSA CERS6 CPT2 CS DHDDS ECHS1 FOLR2 GAA GBE1 GGT1 GPX1 HADHB HMGCL HSD17B6 MMUT OGG1 PDHA1 PLCE1 SDHA SDHB SDHC SLC25A1 SLC39A8 SOAT1 SORD SULT1E1 TYMP	1376 1431 1890 1892 217 2350 253782 2548 2632 2678 2876 3032 31 3155 353 410 4594 4968 51 51196 5160 55750 6389 6390 6391 64116 6576 6646 6652 6783 79947 8630	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0080072	intestinal pseudo-obstruction Aliases: Chronic intestinal pseudo-obstruction neuronal intestinal dysplasia	PTEN	5728	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050754	ataxia with oculomotor apraxia type 1	IDH1 OGG1 PARP1 SDHA STS	142 3417 412 4968 6389	Homo sapiens (human)	DisGeNET
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:0110843	xeroderma pigmentosum group A Aliases: XP group A XP1 XPA xeroderma pigmentosum 1 xeroderma pigmentosum complementation group A	CAT COMT CYP1A1 CYP1B1 HPGDS HPRT1 OGG1 PARP1 PTEN PTGS2 SMUG1 TALDO1 XYLT2	1312 142 1543 1545 23583 27306 3251 4968 5728 5743 64132 6888 847	Homo sapiens (human)	DisGeNET DisGeNET
DOID:5563	malignant teratoma Aliases: Immature teratoma Teratoma, malignant, NOS malignant Extragonadal teratoma primary malignant extragonadal teratoma	ACAT1 ALPP DHCR24 ENO2 FMOD FUT1 GFRA1 ME1 MRC1 PGM1 PSMD10 PTEN SMUG1	1718 2026 2331 23583 250 2523 2674 38 4199 4360 5236 5716 5728	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0111529	familial multiple nevi flammei Aliases: CMC congenital capillary malformations familial multiple port-wine stains	CYP1B1 ICAM1 KLRB1 MAG PIK3CA PIK3CB PIK3CD PIK3CG	1545 3383 3820 4099 5290 5291 5293 5294	Homo sapiens (human)	DisGeNET DisGeNET
DOID:6406	double outlet right ventricle Aliases: Dextrotransposition of aorta Double outlet right ventricle with subpulmonary ventricular septal defect Taussig-Bing syndrome or defect	CERS1 CFC1 COMT DGCR2 GPC3 NT5E PTEN PTGS2 TMEM260 UGCG	10715 1312 2719 4907 54916 55997 5728 5743 7357 9993	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:5463	cochlear disease	TNF	7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:11252	microcytic anemia	ACO1 BDH2 CACNA2D3 CAT CD55 HJV IDUA LALBA LPIN2 PLA2G4A PLA2G6 SMPD1 SRD5A3	148738 1604 3425 3906 48 5321 55799 56898 6609 79644 8398 847 9663	Homo sapiens (human)	DisGeNET DisGeNET
DOID:9256	colorectal cancer	ABO ACACA ACACB ACADM ACAN ACAT1 ACE ACHE ACLY ACO2 ACOT7 ACOX1 ACSBG1 ACSL1 ACSL4 ACSL5 ACSS2 ACYP2 ADH1B ADH1C ADH7 AFMID AGL AKR1A1 AKR1B10 AKR1B1 AKR1C1 AKR1C3 AKT1 AKT2 ALDH1A3 ALDH1B1 ALDH2 ALDH3A1 ALDH7A1 ALDOB ALOX12 ALOX12B ALOX15 ALOX15B ALOX5 ALPI ALPP AMACR AMDHD2 AMT ANXA4 ANXA5 ANXA7 ANXA9 APRT ARSA ARSB ART1 ASAH1 ASAH2 ATP6AP2 ATP6V1A ATRNL1 B3GALT4 B3GALT5 B3GAT1 B3GNT6 B3GNT7 B3GNT8 B3GNTL1 B4GALNT3 B4GALT1 B4GALT2 B4GALT3 B4GALT5 B4GALT6 BAAT BPHL BRAF BST2 C1GALT1 C1GALT1C1 CA4 CACNA2D1 CACNA2D2 CALR CAT CBR1 CD109 CD14 CD177 CD209 CD248 CD33 CD38 CD44 CD55 CDH13 CDS1 CEACAM5 CEACAM6 CEACAM7 CEMIP CERS4 CERS5 CERS6 CHAT CHGA CHI3L1 CHIT1 CHKA CHPF2 CHPT1 CHST4 CHST7 CHST8 CHSY1 CHSY3 CLC CLEC3A CMAS CNTN1 CNTN4 COG8 COMT CPM CPO CPT1A CPT2 CSGALNACT1 CTBS CTSA CYB5R1 CYB5R3 CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP1B1 CYP24A1 CYP27B1 CYP2B6 CYP2C19 CYP2C9 CYP2E1 CYP2R1 CYP3A4 CYP3A5 CYP46A1 CYP4F3 CYP7A1 CYP7B1 DAG1 DCN DEGS1 DEGS2 DGKB DGKE DGKG DGKZ DHCR24 DHCR7 DHDDS DHRS11 DLD DPAGT1 DPEP1 DSEL EBP EFNA1 ELOVL5 ENO1 ENOSF1 ENPP1 ENPP3 ENPP7 EXTL3 FADS1 FADS2 FASN FBP1 FCGR3B FCN1 FCN2 FH FMOD FOLR1 FOLR2 FUCA1 FUT1 FUT2 FUT3 FUT4 FUT5 FUT6 FUT7 FUT8 FUT9 G6PD GAD1 GAD2 GALK1 GALM GALNS GALNT11 GALNT12 GALNT14 GALNT15 GALNT1 GALNT3 GALNT4 GALNT6 GALNT7 GAPDH GAS1 GCDH GCLC GCNT1 GCNT2 GCNT3 GCNT7 GDPD5 GFRA1 GFRA2 GGT1 GLB1 GLO1 GLTP GMDS GML GOLPH3 GPAA1 GPC1 GPC3 GPC6 GPI GPLD1 GPNMB GPX1 GPX2 GPX3 GUSB H6PD HADHB HAS2 HAS3 HEXB HIBCH HK1 HK2 HK3 HKDC1 HMGCS1 HMGCS2 HMMR HPGDS HPRT1 HPSE HSD11B1 HSD11B2 HSD17B1 HSD17B2 HSD17B4 HSD17B7 HSPG2 HYAL1 HYAL2 ICAM1 ICAM5 IDH1 IDH2 IDUA IGF2R IL18R1 IL1R1 IL1RL1 IMPA1 INPP1 INPP4B INPP5D INPPL1 ISYNA1 ITPKC KL KLRC1 KLRK1 L1CAM LAYN LCT LDHA LDHB LGALS12 LGALS1 LGALS3 LGALS4 LGALS8 LGALS9 LIPC LMAN1 LPCAT2 LPCAT4 LPIN1 LPL LTA4H LTC4S LY6G6D LYNX1 LYPD5 MACROD1 MACROD2 MANBA MASP2 MBD4 MBL2 MCAT ME1 MECR MELTF MGAT4A MGLL MICA MINPP1 MMP25 MMUT MPG MRC1 MSLN MTAP MTM1 MTMR3 MTMR7 MUTYH NAAA NAMPT NANP NCAM1 NDST4 NEIL1 NEIL2 NEU1 NEU3 NT5E NTHL1 NTNG1 OGA OGDH OGDHL OGG1 OGT OLR1 OVGP1 PARG PARP1 PARP4 PARP6 PARP8 PCCA PCCB PCK1 PCYT1A PCYT1B PDHX PDIA3 PFKFB3 PGAM1 PGK1 PGM1 PGM5 PGP PIGF PIGK PIGN PIGO PIGU PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1A PKD1 PKD1L2 PKLR PKM PLA2G10 PLA2G15 PLA2G1B PLA2G2A PLA2G2D PLA2G3 PLA2G4A PLA2G6 PLA2G7 PLAAT3 PLAUR PLB1 PLCB1 PLCD1 PLCE1 PLCG1 PLCH1 PLD1 PLD2 PLD4 PLEKHA8 PMM2 PNP PNPLA2 POC1B-GALNT4 POFUT1 POGLUT1 PPP1R3A PPP1R3C PPT1 PRG2 PRKAA2 PRNP PRPS1 PSMD10 PTEN PTGDS PTGES2 PTGES PTGIS PTGS1 PTGS2 RECK REG1B RENBP RGMB RGN RPE RPIA RPN2 RTN4R RTN4RL2 SCD SDC1 SDC2 SDC4 SDCBP2 SDHB SDHC SDHD SELE SELL SELP SGMS1 SGMS2 SGPL1 SHMT1 SHMT2 SI SIGLEC6 SIGLEC7 SIGLEC9 SIRT2 SIRT4 SIRT6 SLC17A5 SLC26A2 SLC2A2 SLC2A3 SLC2A4 SLC2A5 SLC33A1 SLC35A2 SLC35G1 SLC39A8 SLC3A1 SMC3 SMPD1 SMUG1 SOAT1 SORD SPHK1 SPHK2 SQLE SRGN ST3GAL4 ST3GAL6 ST6GAL1 ST6GALNAC1 ST6GALNAC2 ST8SIA1 ST8SIA4 STS STT3A SULF1 SULF2 SULT1E1 SYNJ2 TDG TIGAR TKT TKTL1 TKTL2 TLR2 TM7SF2 TMED3 TMED6 TMED9 TMTC1 TNKS TP53 TPI1 TPST1 TUSC3 TYMP UGT1A10 UGT1A1 UGT1A4 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UGT2B15 UGT2B17 UGT2B28 UGT2B7 UGT3A2 ULBP2 UMPS UNG UPP1 VCAM1 VCAN VNN1 VTCN1	10026 100507436 100528030 10082 1012 10135 10143 10159 10164 10232 10317 10327 1040 10402 10457 1048 10610 10682 10690 10724 10747 10825 10855 10858 1087 1103 1113 11145 1116 1118 1119 11226 11320 11332 11343 114780 117248 1178 120227 122618 123099 125 125061 126 1272 128869 130589 130749 131 1312 135228 1368 1374 1376 140687 140733 140838 142 143 143903 1462 146456 146712 1486 151056 152330 1543 1544 1545 1555 1557 1559 1571 1576 1577 1581 1586 1588 1591 159371 1594 1604 1605 1607 1608 1634 1636 1645 166929 167127 1717 1718 1727 1738 176 178 1798 1800 1836 1890 192134 1942 2023 207 208 2137 217 218 2180 2182 219 2194 220 2203 2215 2219 2220 2271 22854 22856 229 22914 22933 22934 23007 231 23175 23205 23213 23236 2331 23409 23423 2348 2350 23509 23556 23583 23600 23659 239 240 242 246 247 248 250 2517 2523 2524 2525 2526 2527 2528 2529 252969 2530 253782 2539 254531 2571 2572 2584 2588 2589 2591 259230 2597 26033 2619 26275 26279 2639 2650 26503 2651 2674 2675 2678 2683 27036 27087 27111 27163 27180 2719 2720 2729 27306 27349 2739 275 2762 2765 28 2817 2821 2822 283358 283871 284348 285704 2876 2877 2878 28992 29071 2923 2990 3032 3037 3038 307 3074 308 30835 3098 3099 31 310 3101 3157 3158 3161 32 3251 3290 3291 3292 3294 3295 3339 3373 337876 3383 339221 34 3417 3418 3425 3482 349667 353 3554 3612 3628 3635 3636 3703 374907 38 3821 3897 3938 3939 3945 3956 3958 3960 3964 3965 3990 3992 3998 4023 4048 4051 4056 410 411 412 4126 4153 417 4199 4241 427 43 4350 4360 4507 4534 4594 4595 4680 4684 47 4758 4860 4907 4913 4967 4968 4973 50 501 5016 50487 5095 5096 51 51005 5105 51102 51196 51228 5130 51477 51478 51548 5167 5169 51703 51706 51809 5209 5223 523 5230 5236 5239 5281 5289 5290 5291 5293 5294 5310 5313 5315 5319 5320 5321 5329 5333 5335 5337 5338 5373 54480 54490 54575 54576 54577 54578 54600 54657 54658 54732 5476 54947 5506 5507 5538 5552 5553 55556 5563 55753 55790 55808 55902 55907 55959 5621 5631 56548 56624 56848 56913 56965 56983 56994 570 57016 57103 57104 57124 57126 5716 57214 5728 5730 5740 5742 5743 58530 5968 5973 60481 6120 6185 6319 6382 6383 6385 6390 6391 63917 6392 6401 6402 6403 64083 64116 64377 64386 64579 6470 6472 6476 6480 6484 6489 65078 6514 6515 6517 6518 6519 66004 6609 6646 6652 670 6713 673 6783 684 6996 7086 7087 7097 7108 7157 7167 7355 7364 7366 7367 7372 7374 7378 7412 762 781 7903 79154 7941 79603 79623 79661 79668 79679 79695 7991 79947 80142 80201 80271 80328 8050 811 81544 8277 83857 8394 8398 8399 84076 8416 8434 84342 8460 847 84720 84725 8473 8505 8525 8526 85329 8560 8644 8658 8692 8693 8703 8704 8705 873 8733 8809 8821 8871 8876 8877 8879 8897 8930 91012 9104 9108 9126 9173 9197 92126 9245 9254 929 93010 9331 9334 9365 9415 9420 945 946 9468 952 9536 9562 9563 960 98	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:1752	ocular melanoma Aliases: eye melanoma intraocular melanoma melanoma of eye	ASAH1 CD177 CYP24A1 CYP27B1 PNPLA2 SDHD	1591 1594 427 57104 57126 6392	Homo sapiens (human)	DisGeNET
DOID:2218	blood platelet disease Aliases: Thrombocytopathy platelet disorder	ACHE HPSE KDSR PLA2G4A	10855 2531 43 5321	Homo sapiens (human)	DisGeNET
DOID:7187	subacute lymphocytic thyroiditis	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:5769	verruciform xanthoma of skin Aliases: Cutaneous Verruciform Xanthoma Verruciform xanthoma	NSDHL	50814	Homo sapiens (human)	DisGeNET
DOID:0060041	autism spectrum disorder	ABAT ACACA ACAN ACSM3 ALDH1A3 AMT AMY1A AMY1B AMY1C ARSA ARSD B3GLCT BST1 CAT CD38 CDH13 CHAT CLEC7A CNTN2 CNTN4 CNTN5 CNTN6 COMT CS CYP11A1 CYP11B1 CYP11B2 CYP19A1 CYP1A2 CYP1B1 CYP27A1 CYP2C19 CYP2E1 CYP2R1 DGCR2 DHCR24 DHCR7 ELOVL2 ENO2 EPHX2 EXT1 FADS1 FADS2 FH FOLR1 FOLR2 GAD1 GAD2 GALNT17 GLO1 GLUL HAGH HPGDS HTR2A IDS IL1RAP IL1RAPL1 IL1RAPL2 L1CAM LDHB LYZ MACROD2 MBOAT7 MRC1 NCAM1 NDST1 NDST2 NDST3 NDST4 NTM OGG1 PAFAH1B1 PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PKD2 PLA2G12A PLA2G4C PLAUR PLCB1 POMGNT1 PTEN PTGES3 PTGES PTGS1 PTGS2 RTN4R SCD SDC4 SLC25A12 SLC2A3 SLC33A1 SLC35A3 SOAT1 ST8SIA2 STS TM7SF2 TPI1 UGT1A1 UPP2	1012 10728 1103 11141 120227 1312 140733 1431 145173 151531 152330 1544 1545 1557 1571 1583 1584 1585 1588 1593 1717 1718 176 18 2026 2053 2131 220 2271 23236 23443 2348 2350 2571 2572 26280 27255 27306 2739 275 2752 276 277 278 3029 31 3340 3356 3423 3556 3897 3945 3992 4069 410 412 414 4360 4684 4968 5048 50863 5130 5290 5291 5293 5294 5311 5329 53942 54658 54898 55624 5728 5742 5743 6296 6319 6385 64409 64579 64581 65078 6515 6646 683 6900 7108 7167 79143 8128 81579 847 8509 8604 8605 9197 9348 9415 952 9536 9993	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:13186	megaesophagus	AGA CALR ECI1 FUT3 GMPPA	1632 175 2525 29926 811	Homo sapiens (human)	DisGeNET
DOID:9952	acute lymphoblastic leukemia Aliases: ALL acute lymphoblastic leukaemia acute lymphocytic leukaemia precursor lymphoblastic lymphoma/leukemia	ABO ACSS2 AKR1B1 AKR1C3 ALPI ALPP ANXA5 APRT B3GAT1 CALR CAT CD14 CD1D CD22 CD33 CD38 CD44 CD48 CD55 CD72 CDH13 CEACAM5 CEACAM6 CEACAM7 CEL CERS6 CHI3L1 CHST9 CLEC12A CNTFR COLEC10 CSPG4 CYP1A1 CYP1A2 CYP1B1 CYP2B6 CYP2C19 CYP2C8 CYP2E1 CYP3A4 CYP3A5 CYP4F3 EBP EFNA5 ENO2 EXT1 FADS1 FH FUT4 G6PD GAD1 GAPDH GGT1 GML GPI GPX1 HK1 HMMR HPGDS HPRT1 HPSE2 HPSE HS3ST4 ICAM1 IDH1 IDH2 IDUA IL18R1 IL1RL1 INPP5D ISYNA1 KLRK1 LGALS1 LGALS3 LIPA LPL LSS MBL2 MOGS MTAP NAAA NAMPT NCAM1 NT5E PARP9 PGP PIGL PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2A PLA2G15 PLCG2 PNP PNPLA3 PRKAA2 PRPS1 PTEN PTGS2 SACM1L SCD SELE SFTPD SHMT1 SLC27A5 SMUG1 SOAT1 SPHK2 ST8SIA6 UGT1A1 UMOD UNG	1012 10135 1048 1056 10584 10682 10855 1087 10998 1116 1271 1464 1543 1544 1545 1555 1557 1558 1571 1576 1577 160364 1604 1946 2026 2131 2271 22908 22914 231 23583 23659 248 250 2526 253782 2539 2571 2597 2678 27087 27163 27306 2765 28 2821 283871 2876 308 3098 3161 3251 3383 338596 3417 3418 3425 353 3635 3956 3958 3988 3992 4023 4047 4051 4153 4507 4680 4684 4860 4907 51477 5290 5291 5293 5294 5305 5336 54658 5563 55902 5631 56848 5728 5743 60495 6319 6401 6441 6470 6646 7369 7374 7841 80339 811 83539 83666 847 8644 8809 912 9173 929 933 945 9487 952 960 962 971 9951	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:4239	alveolar soft part sarcoma	CD38 COG8 TMED6	146456 84342 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:0110046	Alzheimer's disease 13 Aliases: AD13 Alzheimer disease 13 Alzheimer's disease 13, late onset	ABO ACACA ACADVL ACAT1 ACE ACHE ACO1 ACO2 ACOT7 ACOT8 ACSL6 ACSS2 AGPS AGRN AKR1A1 AKR1C2 AKR1C4 ALDH2 ALDH7A1 ALOX12 ALOX5 ALPI ALPP ANXA5 APRT ARSA ASAH1 ATRNL1 B3GALT4 B3GAT1 BCAN BST1 CALR CAT CD14 CD177 CD209 CD33 CD38 CD44 CD55 CD74 CDH13 CEACAM5 CFC1 CH25H CHAT CHI3L1 CHIT1 CLC CLEC16A CLEC1B CLEC7A CLN5 CNTN1 CNTN2 COG5 COLGALT2 COMT CPO CPT1A CRYL1 CS CSPG4 CTNS CYP11A1 CYP17A1 CYP19A1 CYP1A2 CYP27A1 CYP2B6 CYP2C9 CYP2J2 CYP3A4 CYP46A1 CYP7B1 CYP8B1 DCN DEGS1 DGKQ DHCR24 DHRS11 DLD DLST DPEP2 EDEM2 EFNA5 ENO1 ENO2 ENPP2 EPHX2 FASN FBXO2 FCGR3B FCN2 FDPS FOLR2 G6PD GAD1 GAD2 GALNS GAPDH GAPDHS GBA1 GFRA1 GGT1 GLB1 GLO1 GLUL GNE GNPAT GNPDA2 GOLPH3 GPAA1 GPC1 GPC6 GPI GPNMB GPX1 GTDC1 GUSB HAS1 HAS3 HK1 HMGCS2 HPGDS HPSE2 HPSE HS3ST1 HSD11B1 HSD17B1 HSD17B4 HSD17B6 HSD17B7 HSPG2 HYI ICAM1 IDH1 IDH2 IGF2R IL1R1 IL1RAP IL1RL1 IMPA1 INPP5D INPP5K INPPL1 ITPKB KL KLRC1 L1CAM LCAT LCT LDHA LGALS3 LGALS4 LGALS9 LIPA LIPC LIPG LPL LTC4S LYZ LYZL4 MAG MASP1 MBL2 MDH2 MELTF MGAT3 MGLL MICA MMUT MOGAT3 MPG MPI MRC1 NAAA NAMPT NANS NCAM1 NEU1 NPL NT5E OGA OGDH OGDHL OGG1 OGT OLR1 PAFAH1B2 PARP1 PC PCK1 PCYT1A PCYT1B PEMT PFKFB3 PGD PGP PI4KA PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIKFYVE PKM PLA2G15 PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLA2G7 PLAUR PLB1 PLCB1 PLCG2 PLD1 PLD2 PLD3 PLPP4 PMM2 PNP PNPLA2 PNPLA7 PPT1 PRG2 PRKAA2 PRNP PTDSS1 PTEN PTGDS PTGES2 PTGES3 PTGES PTGS1 PTGS2 RENBP RGN RTN4R SCD5 SCD SCP2 SDC2 SDC3 SDCBP2 SFTPA1 SFTPC SGMS2 SGSH SI SIGLEC7 SIRT2 SIRT6 SLC2A3 SLC2A4 SLC33A1 SLC35A1 SLC35A2 SMPD2 SMPD3 SMUG1 SOAT1 SPHK1 SPHK2 SQLE ST3GAL4 ST6GAL1 ST8SIA1 STS SUCLA2 SUCLG2 SYNJ1 TIGAR TKT TM7SF2 TMED9 TPI1 UGCG UGT1A1 UMOD UNG VCAM1 VCAN	10005 10020 100507436 10082 1012 10135 10327 10400 10457 10466 1048 10559 10724 10728 10855 10858 1103 1109 1116 1118 11332 11343 1178 1203 1272 130749 1312 131375 132789 1374 142 1431 1462 1464 1497 151056 1544 1555 1559 1573 1576 1582 1583 1586 1588 1593 1604 1609 1634 1636 1646 166929 1718 1738 1743 1946 196051 200576 2023 2026 2053 217 2194 2215 2220 2224 22933 23127 23236 23274 23305 2350 23583 23646 23659 239 240 248 250 2539 2571 2572 2588 2597 26033 26232 2629 26330 2674 2678 27036 27087 27111 27163 2720 27306 2739 2752 28 2817 2821 283871 2876 2990 3036 3038 308 30835 3098 31 3158 3290 3292 3295 3339 3383 3417 3418 346606 3482 353 3554 3556 3612 3635 3636 37 3707 375775 375790 38 3821 3897 3931 3938 3939 3958 3960 3965 3988 3990 4023 4056 4069 4099 410 412 4153 4191 4241 4248 427 43 4350 4351 4360 4594 4684 4758 48 4860 4907 4967 4968 4973 50 501 5049 5091 5105 51084 51266 5130 51478 51548 5168 51763 5209 5226 5289 5290 5291 5293 5294 5297 5315 5319 5320 5321 5329 5336 5337 5338 5373 54187 54658 54732 5538 55512 5553 5563 55741 55753 55902 55997 5621 5648 56848 57103 57104 57126 5728 5730 5742 5743 5973 60495 6319 6342 63827 6383 64083 64174 6440 6448 64581 6476 6480 6484 6489 65078 6515 6517 653509 6610 6646 6713 683 6900 7086 7108 7167 7355 7357 7369 7374 7412 79154 7941 79712 79966 80142 80896 811 81888 8398 8443 847 8473 8540 8560 8630 8705 8733 8801 8803 8867 8877 9023 9104 9173 9197 929 9365 9388 9420 945 9468 952 9536 960 9672 972 9791 9957	Homo sapiens (human)	DisGeNET
DOID:0060575	3MC syndrome 1	COLEC11 MASP1	5648 78989	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:7134	esophagus small cell carcinoma Aliases: Oat cell carcinoma of esophagus Oat cell carcinoma of oesophagus oesophagus small cell carcinoma	PARP1 PTEN	142 5728	Homo sapiens (human)	DisGeNET

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