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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 **4701 - 4725** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:0110044	Alzheimer's disease 11 Aliases: AD11 Alzheimer disease 11 Alzheimer's disease 11, 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:0110447	dilated cardiomyopathy 1DD Aliases: CMD1DD	ACADVL ACE BDH1 CHKB CPT2 DAG1 DOLK FASN FKRP FKTN GLB1 GPX1 HACD1 HADH HADHA HADHB HJV HMGCL HPRT1 LDHA LGALS3 LPL MDH1 MICA MTM1 NAMPT NCAM1 NDUFAB1 PCYT1A PGM1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G7 POMT2 RENBP SDHA SDHD SLC2A10 SLC2A4	100507436 10135 1120 1376 148738 1605 1636 2194 2218 22845 2720 2876 29954 3030 3032 3033 3155 3251 37 3939 3958 4023 4190 4534 4684 4706 5130 5236 5290 5291 5293 5294 5973 622 6389 6392 6517 79147 7941 81031 9200	Homo sapiens (human)	DisGeNET
DOID:0080544	hyper IgM syndrome Aliases: HIGM hyperimmunoglobulin M syndrome immunodeficiency with hyper-IgM	CHI3L1 FCER2 MRC1 UNG	1116 2208 4360 7374	Homo sapiens (human)	DisGeNET
DOID:219	colon cancer	ACACA ACAN ACAT1 ACE ACHE ACLY ACSL1 ACSL4 ACSS2 ADH1B ADH1C AFMID AGL AKR1B10 AKR1B1 AKR1C1 AKR1C3 AKT1 ALDH1A3 ALDH1B1 ALDH2 ALDH3A1 ALDH7A1 ALG1 ALOX12B ALOX15 ALOX5 ALPP AMACR ANXA5 APRT ARSA ASAH1 ATRNL1 B3GALT5 B3GNT7 B3GNT8 B3GNTL1 B4GALNT3 BAAT BAD C1GALT1 C1GALT1C1 CA4 CACNA2D1 CALR CAT CBR1 CD109 CD248 CD44 CD55 CDH13 CEACAM5 CEACAM6 CEACAM7 CEMIP CERS4 CERS5 CHAT CHGA CHI3L1 CHKA CHPT1 CHST4 CLEC3A COMT CSGALNACT1 CTBS CYB5R1 CYB5R3 CYP17A1 CYP1A1 CYP1A2 CYP1B1 CYP24A1 CYP27B1 CYP2E1 CYP2R1 CYP3A4 CYP4F3 CYP7A1 CYP7B1 DAG1 DCN DGKB DGKE DGKZ DHCR24 DHCR7 DHDDS DLD DPEP1 EBP ELOVL5 ENO1 ENPP3 ENPP7 FADS1 FADS2 FASN FBP1 FDPS FH FOLR1 FUT1 FUT4 FUT6 FUT7 G6PD GALNT12 GALNT4 GALNT6 GAPDH GCNT2 GCNT3 GLB1 GLO1 GMDS GOLPH3 GPC1 GPI GPLD1 GPX1 GPX2 GPX3 GSK3B GUSB HAS3 HEXB HK2 HMGCS1 HMGCS2 HMMR HPGDS HPRT1 HPSE HS3ST2 HSD11B2 HSD17B4 HSD17B7 HSPG2 HYAL2 ICAM1 IDH1 IDUA IGF2R IL1R1 IMPA1 INPP4B INPP5D INPPL1 ISYNA1 KL KLRK1 L1CAM LAYN LDHA LDHB LGALS12 LGALS1 LGALS3 LGALS4 LGALS8 LGALS9 LIPC LPIN1 LPL LYPD5 MACROD2 MAPK14 MBD4 MBL2 ME1 MGAT5 MGLL MICA MINPP1 MMP25 MRC1 MTM1 MTMR3 MUTYH NAMPT NEU3 NTHL1 NTNG1 OGA OGG1 OLR1 PARP1 PARP4 PCYT1A PCYT1B PFKFB3 PGK1 PIGU PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1A PKM PLA2G10 PLA2G15 PLA2G1B PLA2G2A PLA2G2D PLA2G3 PLA2G4A PLA2G6 PLA2G7 PLAUR PLB1 PLCB1 PLCG1 PLCH1 PLD2 PLD4 PLEKHA8 PLPP3 PNP PNPLA2 POGLUT1 PRKAA1 PRKAA2 PSMD10 PTEN PTGDS PTGES PTGIS PTGS1 PTGS2 RECK REG1B RENBP RGN RPE RPIA SCD SDC1 SDC2 SDC4 SDHA SDHB SDHC SELE SELL SGMS2 SGPL1 SHMT1 SHMT2 SIGLEC7 SIRT2 SIRT6 SLC17A5 SLC26A2 SLC2A2 SLC2A3 SLC2A4 SLC2A5 SLC35A2 SMPD1 SMUG1 SOAT1 SPHK1 SPHK2 SRGN ST6GAL1 ST6GALNAC1 STS STT3A SULF1 SULT1E1 SYNJ2 TDG TIGAR TKT TKTL1 TKTL2 TM7SF2 TMED3 TMED9 TMTC1 TNFRSF10C TNKS TUSC3 TYMP UGT1A1 UGT1A6 UGT1A7 UGT1A9 UGT2B17 ULBP2 UMPS UNG UPP1 VCAM1 VCAN VNN1	100507436 1012 10135 10143 10164 10317 1048 10682 10724 10825 10855 1087 1103 1113 1116 1119 11226 11343 120227 122618 125 125061 126 128869 1312 135228 140733 142 143 1432 143903 1462 146712 1486 151056 1543 1544 1545 1571 1576 1581 1586 1591 1594 1604 1605 1607 1634 1636 1645 166929 1717 1718 1727 1738 176 178 1800 1836 1890 2023 207 217 218 2180 2182 219 2194 220 2203 2224 2271 22854 22914 22933 22934 23007 231 23175 23213 23236 23423 2348 23583 23600 23659 240 242 246 250 2523 2526 2528 2529 2539 2597 26033 26279 26503 2651 27036 2720 27306 2739 2762 2817 2821 2822 283358 284348 2876 2877 2878 29071 2932 2990 3038 3074 308 3099 31 3157 3158 3161 3251 3291 3295 3339 3383 339221 3417 3425 3482 353 3554 3612 3635 3636 3703 374907 38 3897 3939 3945 3956 3958 3960 3964 3965 3990 3992 4023 4051 410 412 4153 4199 4249 427 43 4360 4534 4595 4680 47 4860 4913 4968 4973 501 50487 5130 51477 51478 51548 5169 51706 5209 5230 5289 5290 5291 5293 5294 5315 5319 5320 5321 5329 5335 5338 54577 54578 54600 54658 54732 5552 5562 5563 55790 55808 55902 56052 56848 56913 56983 56994 570 57016 57103 57104 57124 5716 572 57214 5728 5730 5740 5742 5743 5968 5973 60481 6120 6319 6382 6383 6385 6389 6390 6391 6401 6402 64083 64386 6470 6472 6480 6514 6515 6517 6518 6609 6646 6783 6996 7086 7108 7355 7367 7372 7374 7378 7412 762 781 7941 79603 79695 7991 79947 80328 811 8277 83857 8394 8398 8399 84076 8434 847 84725 8525 8526 85329 8613 8644 8658 8692 8693 873 8794 8821 8871 8876 8877 8879 8897 8930 91012 9104 9245 93010 9365 9415 9420 9468 9536 9562 960 9956	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:3310	atopic dermatitis Aliases: Atopic neurodermatitis Besnier's prurigo allergic dermatitis atopic eczema	ABO AKR1C3 ALDH7A1 ALOX12B CD14 CD1D CD48 CD55 CERS3 CERS4 CHI3L1 CHST3 CHST8 CLEC10A CLEC16A CLEC7A CYP1A1 CYP24A1 CYP27A1 CYP27B1 ELOVL3 ELOVL6 ENO1 FADS2 FAR2 FCER2 GLB1 HAS3 HPGDS HSD11B1 ICAM1 IL18R1 IL1R1 IL1RL1 ITLN1 LGALS1 MBL2 MGLL NAAA NPL OGA PGD PGM3 PLA2G1B PLA2G2E PLA2G4D PLAUR PLB1 PLD3 PTGDS PTGS2 SELE SELP SIGLEC7 SLC2A2 SLC35G1 SMPD2 SOAT1 TLR2 TLR4 TNF TPI1 UGT1A9 VCAM1 VNN1 VNN2	10462 10724 1116 11343 151056 1543 1591 1593 159371 1594 1604 2023 204219 2208 23274 23646 242 27036 27163 2720 27306 28 283748 3038 30814 3290 3383 3554 3956 4153 501 5226 5238 5319 5329 54600 55600 55711 5730 5743 6401 6403 64377 64581 6514 6610 6646 7097 7099 7124 7167 7412 79071 79603 80896 83401 8644 8809 8875 8876 912 9173 929 9415 9469 962	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:2846	bruxism Aliases: Bruxism - teeth grinding Grinding teeth Teeth grinding sleep related bruxism	PGAP3	93210	Homo sapiens (human)	DisGeNET
DOID:7960	malignant spiradenoma Aliases: malignant eccrine spiradenoma	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:11193	syndactyly Aliases: symphalangism symphalangy webbing of digits	ACSL3 B3GLCT CHSY1 FIG4 MAN1B1 MMUT PIK3CA PTDSS1	11253 145173 2181 22856 4594 5290 9791 9896	Homo sapiens (human)	DisGeNET
DOID:83	cataract	ACE ACSM3 AGA AGK AKR1B1 ALDH3A1 ALDH6A1 ALDH7A1 ALDOB ALG2 ALG8 ARSA ARSG ATP6V1A B3GALNT2 B3GLCT B4GALNT1 B4GAT1 CA4 CALR3 CAT CD14 CHPT1 CHST1 COG4 COL9A2 COMT CPT2 CRPPA CRYL1 CYP19A1 CYP27A1 CYP51A1 CYP7B1 DAG1 DHDDS DPAGT1 EBP EFNA5 EOGT FDFT1 FH FIG4 FKRP FKTN G6PD GALK1 GALT GBA2 GCLC GCNT2 GLA GMPPB GNPAT GPX1 HGSNAT HPGDS HSPG2 IDH3A IDH3B INPP5E INPP5K KDSR KLRB1 LARGE1 LSS NAGA NEU1 OCRL OGG1 PCYT1A PIK3C2A PIK3CA PIK3CB PIK3CD PIK3CG PLA2G4A PLB1 PLOD3 PMM2 PNPLA6 POMGNT1 POMGNT2 POMK POMT1 POMT2 PTEN PTGS2 RGN RXYLT1 SC5D SDHB SDHC SLC2A3 SLC33A1 SMC3 SORD SRD5A3 ST3GAL4 SUMF1 TKFC VCAN XYLT2	10329 10585 10682 10908 11041 125972 1298 1312 1376 138050 145173 1462 148789 151056 1588 1593 1595 1605 1636 175 1798 1946 218 2218 2222 2271 229 22901 231 2531 2539 2583 25839 2584 2592 26007 2651 2717 2729 27306 285203 285362 2876 29925 29954 3339 3419 3420 3820 4047 410 4329 4668 4758 4952 4968 501 51084 5130 51763 523 5286 5290 5291 5293 5294 5321 5373 55624 55750 56623 56994 5728 5743 57704 6296 6309 6390 6391 64132 6484 6515 6652 729920 762 79053 79147 79644 79947 84197 8443 847 84892 8534 85365 8985 9104 9126 9197 9215 929 9420 9896	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0110504	autosomal recessive nonsyndromic deafness 47 Aliases: DFNB47 autosomal recessive deafness 47	ACO2 ACOX1 ARSA CD109 CHSY1 COG4 LRTOMT OTOA OTOG PSAP TECTA	135228 146183 220074 22856 25839 340990 410 50 51 5660 7007	Homo sapiens (human)	DisGeNET
DOID:5052	melioidosis Aliases: Nightcliff gardener's disease Pseudoglanders Whitmore's disease acute and fulminating melioidosis subacute and chronic melioidosis	CALR CD14 HSD17B6 PLAUR SELL STS	412 5329 6402 811 8630 929	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0060181	ischemic colitis	PC PTGS2 SMUG1	23583 5091 5743	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0090070	hypogonadotropic hypogonadism Aliases: congenital idiopathic hypogonadotropic hypogonadism hypogonadotropism isolated congenital gonadotropin deficiency	ACSM3 ADH5 CD44 CD55 CYP17A1 CYP19A1 GAS1 GK GPC1 HJV HS6ST1 HSD17B3 L1CAM MMUT NT5E PMM2 PNPLA6 SEMA7A SMPD3 SOAT1 STS TYMP	10908 128 148738 1586 1588 1604 1890 2619 2710 2817 3293 3897 412 4594 4907 5373 55512 6296 6646 8482 9394 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:11613	hyperandrogenism Aliases: hyperandrogenization syndrome	ACE AKR1C3 CYP11A1 CYP17A1 CYP19A1 CYP21A2 H6PD HSD11B1 HSD17B7 HSD3B2 IL6ST NAMPT PAPSS2 PIK3CA PIK3CB PIK3CD PIK3CG STS UGT2B15	10135 1583 1586 1588 1589 1636 3284 3290 3572 412 51478 5290 5291 5293 5294 7366 8644 9060 9563	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:6195	conjunctivitis	ART4 CD14 IMPA1 LGALS1 MBL2 PLD3	23646 3612 3956 4153 420 929	Homo sapiens (human)	DisGeNET DisGeNET
DOID:12140	Chagas disease Aliases: Chagas' disease chagas' disease with digestive system involvement chagas' disease with nervous system involvement chagas' disease with other organ involvement	ABO ACE ACHE ALOX5 CALR COLEC11 CYP2B6 CYP51A1 FCN2 FDPS G6PD GCK GLUL LGALS3 LGALS9 MASP2 MBL2 NT5E PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PLCB1 PLCB4 PNP PRG2 PTGS2 RPIA SDC4 SIRT2 SMPD1 SOAT1 STS TPI1	10747 142 1555 1595 1636 2220 2224 22933 22934 23236 240 2539 2645 2752 28 3958 3965 412 4153 43 4860 4907 5290 5291 5293 5294 5332 5553 5743 6385 6609 6646 7167 78989 811	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:9123	eczema herpeticum Aliases: Herpes simplex dermatitis of eyelid Herpes simplex eyelid dermatitis Herpes simplex virus dermatitis herpes simplex dermatitis herpes simplex virus eyelid dermatitis	CD14 FCGR3B	2215 929	Homo sapiens (human)	DisGeNET
DOID:0110582	autosomal dominant nonsyndromic deafness 58 Aliases: DFNA58 autosomal dominant deafness 58	ACO2 ACOX1 ARSA CD109 CHSY1 COG4 LRTOMT OTOA OTOG PSAP TECTA	135228 146183 220074 22856 25839 340990 410 50 51 5660 7007	Homo sapiens (human)	DisGeNET
DOID:0050807	Kahrizi syndrome Aliases: KHRZ intellectual disability, Kahrizi type intellectual disability-cataract-coloboma-kyphosis syndrome	SRD5A3	79644	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0050949	autosomal recessive hypophosphatemic rickets	ENPP1 GALNT3 IDUA	2591 3425 5167	Homo sapiens (human)	DisGeNET DisGeNET
DOID:12978	Plasmodium vivax malaria Aliases: Malaria by Plasmodium vivax Vivax Malaria	ABO ACOT7 CD55 CYP4F3 G6PD GPI HPGDS PGD PGM1	11332 1604 2539 27306 28 2821 4051 5226 5236	Homo sapiens (human)	DisGeNET
DOID:3241	lipid pneumonia Aliases: Exogenous lipoid pneumonia Lipoid pneumonitis	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:2349	arteriosclerosis Aliases: Arteriosclerotic vascular disease	ABO ACACA ACAN ACAT1 ACE ACER2 ACLY ACOT7 ACSL1 ACSS2 ADH5 AGPAT2 AGXT AKR1B10 AKR1B1 ALDH2 ALDH3A1 ALOX12 ALOX15B ALOX5 ALPL ANXA5 APRT ARSB ARSI ATP6AP2 ATP6V0A2 CACNA2D4 CALR CANX CAT CD14 CD1D CD248 CD44 CD74 CDH13 CEL CH25H CHGA CHI3L1 CHIT1 CHST3 CLEC4E CLEC5A CLEC6A CLEC7A CLEC9A CNTN3 COLEC12 COMT CPT2 CSGALNACT2 CTBS CYP19A1 CYP1A1 CYP1A2 CYP27A1 CYP27B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP2E1 CYP2J2 CYP3A4 CYP3A5 CYP4F2 CYP7A1 DAG1 DCN DGAT1 DHCR24 DLD ELOVL6 ENPP1 ENPP7 EPHX2 FADS1 FADS2 FCGR3B FDPS FMOD FOLR2 FUT3 FUT7 FUT8 GAL3ST1 GCK GLO1 GPI GPIHBP1 GPX1 H6PD HACD4 HAS2 HAS3 HPGDS HPSE HS3ST1 HSD11B1 HSPG2 ICAM1 IDH2 IGF2R IL1RL1 IL6ST INPP5D INPP5K KL KLRK1 LCAT LDHA LEPR LGALS3 LIPA LIPC LIPG LPCAT3 LPL LTA4H LYPLA1 LYZ MBL2 MGLL MICA MMP17 MRC1 MTAP NAAA NAGLU NAMPT NANS NDUFAB1 NEU1 NT5E OGA OGG1 OLR1 PARP1 PARP3 PC PCYT1B PEMT PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G10 PLA2G12A PLA2G15 PLA2G1B PLA2G2A PLA2G2D PLA2G4A PLA2G4C PLA2G6 PLA2G7 PLAUR PLB1 PLPP3 PNP PNPLA2 PNPLA3 PPP1R3B PRKAA2 PRNP PTEN PTGDS PTGES PTGIS PTGS1 PTGS2 RENBP SCD SCP2 SDC1 SDC4 SELE SELL SELP SEMA7A SFTPA1 SFTPA2 SFTPD SGMS1 SGMS2 SGPL1 SIGLEC1 SIGLEC9 SIRT2 SIRT6 SLC17A5 SLC33A1 SLC35A1 SLC39A8 SMPD1 SMPD2 SMPD3 SMUG1 SOAT1 SOAT2 SPHK1 SPHK2 ST3GAL4 ST6GAL1 ST8SIA1 STS SUCLA2 TBXAS1 TLR4 TM7SF2 TPI1 TYMP UMOD VCAM1 VCAN VNN1	10039 100507436 1012 10135 10159 10162 10400 10434 10555 10559 1056 10724 10855 1113 1116 1118 11332 11343 128 1312 1376 142 1462 1486 151056 1543 1544 1555 1557 1558 1559 1571 1573 1576 1577 1581 1588 1593 1594 1605 1634 1636 166929 1718 1738 176 189 1890 2053 217 218 2180 2215 2224 22914 22933 231 2331 2350 23545 23583 23601 23659 239 240 247 249 2525 2529 2530 259230 26253 26279 2645 26503 27163 27180 27306 2739 28 2821 283420 2876 3037 3038 308 31 3290 3339 3383 338328 339221 340075 340485 3418 3482 353 3572 3635 38 3931 3939 3953 3958 3988 3990 3992 401494 4023 4048 4069 411 412 4153 4326 4360 4507 4669 47 4706 4758 4860 4907 4968 4973 5067 5091 51548 5167 51763 5290 5291 5293 5294 5315 5319 5320 5321 5329 54187 55454 55512 5563 55902 5621 56848 57016 57104 57124 5728 5730 5740 5742 5743 5973 6319 6342 6382 6385 6401 6402 6403 64116 6441 64581 6480 6484 6489 653509 6609 6610 6614 6646 6916 7099 7108 7167 729238 7369 7412 79071 7941 79660 80339 81035 811 81579 821 8398 8399 8435 847 8482 8529 8605 8613 8694 8803 8876 8877 8879 9023 912 9173 9197 929 93589 9365 9388 93978 9415 9468 9469 9514 9536 9563 960 972 9957	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:9744	type 1 diabetes mellitus Aliases: IDDM insulin-dependent diabetes mellitus type I diabetes mellitus	ABO ACAN ACE ACHE ACOT7 ACSL1 ADH5 ADIPOQ AGA AGPAT1 AKR1A1 AKR1B1 ALDH2 ALDH3A2 ALOX12 ALOX15B ALOX5 AMY2A ANXA5 APRT B3GAT1 B4GALNT1 B4GALT1 BAAT CAT CBR1 CD14 CD1D CD209 CD38 CD44 CD48 CD74 CDH13 CEACAM5 CEL CEPT1 CHAT CHI3L1 CHST3 CLEC16A CSGALNACT1 CYP21A2 CYP24A1 CYP27A1 CYP27B1 CYP2E1 CYP2R1 CYP7A1 DCN DDOST DGCR2 DHCR7 DLAT EFNA1 ENO2 ENPP1 FADS2 FASN FCER2 FCGR3B FCN2 FKRP FUCA1 FUT2 G6PC1 G6PC2 G6PD GAD1 GAD2 GAL3ST1 GALNT3 GBA3 GCK GLA GLB1 GLO1 GLUL GPI GPX1 GPX3 GYS1 HK1 HK2 HMGCS2 HPGDS HPRT1 HPSE2 HPSE HSD11B1 HSD11B2 HSD17B4 HSPG2 ICAM1 IGF2 IGF2R IL18R1 IL18RAP IL1R1 IL1RL1 INPP5D INPPL1 INS IPPK ISYNA1 KL KLRC3 KLRD1 LDHC LGALS1 LGALS3 LIPC LPL LY6G6D LYPD5 MASP2 MBL2 MGAT1 MGAT5 MICA MIOX NAAA NAMPT NCAM1 OGA PARP1 PDHX PDX1 PFKFB3 PGM1 PGP PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2C PLA2G6 PLA2G7 PNPLA3 PRKAA2 PRKCSH PTEN PTGS2 REG1B RENBP SCD SDC2 SELE SELL SELP SIRT2 SIRT6 SLC2A12 SLC2A2 SLC2A3 SLC2A4 SLC2A8 SLC35A1 SLC35G1 SLC37A4 SLC5A1 SOAT1 ST3GAL4 SULT1E1 TKT TLR2 TLR4 TM7SF2 TNF UGT1A1 UMOD VCAM1 VCAN VTCN1 XYLT1 XYLT2	100507436 1012 10135 10327 10390 1048 10554 10559 1056 10724 10747 10855 1103 1116 11332 120227 128 142 1462 154091 1571 1581 1589 1591 1593 159371 1594 1634 1636 1650 1717 1737 175 176 1942 2026 217 2180 2194 2208 2215 2220 224 22933 231 23274 239 240 247 2517 2524 2538 2539 2542 2571 2572 2583 2591 2645 2683 27087 27163 2717 2720 27306 2739 2752 279 28 2821 283871 284348 2876 2878 2997 29988 308 30835 3098 3099 3158 3251 3290 3291 3295 3339 3383 3481 3482 353 3554 3630 3635 3636 3651 3823 3824 3948 3956 3958 3990 4023 4153 4245 4249 43 4684 51477 51548 5167 5209 5236 5290 5291 5293 5294 54658 55586 5563 55790 5589 570 5728 5743 57733 57818 58530 5968 5973 60495 6319 6383 6401 6402 6403 64131 64132 64768 6484 6514 6515 6517 6523 6646 6783 7086 7097 7099 7108 7124 7369 7412 79147 7941 79679 79837 80339 8050 8398 847 873 8807 8809 912 9173 929 9365 9370 9415 9469 9514 952 960 962 972 9993	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:10017	multiple endocrine neoplasia type 1 Aliases: MEN type I Wermer syndrome Wermer's syndrome	ABO APRT CD109 CYP24A1 FUT4 GAPDH GFRA4 PIK3CA PIK3CB PIK3CD PIK3CG PLCB3 PTEN PYGM RENBP SDHA SDHB SDHC SDHD SMUG1 SORD SULT1E1	135228 1591 23583 2526 2597 28 353 5290 5291 5293 5294 5331 5728 5837 5973 6389 6390 6391 6392 64096 6652 6783	Homo sapiens (human)	DisGeNET DisGeNET

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