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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 **801 - 825** of **4621** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼
DOID:1909	melanoma Aliases: Naevocarcinoma malignant melanoma	ACE ACER3 ACHE ACO1 ACSL3 AKR1B10 ALDH1A3 ALDH3A1 ALDH7A1 ALOX12 ALOX5 ALPI ALPP AMACR ANXA5 ANXA7 ANXA9 APRT ARSB ART3 ASAH1 B3GAT1 B4GALNT1 BRAF BST2 CALR CANX CAT CD14 CD1D CD22 CD248 CD38 CD44 CD74 CDH13 CEACAM5 CEACAM7 CERS2 CERS6 CH25H CHI3L1 CLEC10A CLEC14A CLEC1B CMAS CPT1A CPT1C CRYBG1 CSGALNACT1 CSPG4 CYP19A1 CYP1B1 CYP21A2 CYP24A1 CYP27B1 CYP2B6 CYP2E1 CYP2R1 DBT DERA DGKA DGKI DHCR24 EBP ECHDC1 EDEM1 EFNA1 ELOVL2 ENO2 ENPP1 FASN FCGR3B FDFT1 FDPS FOLR2 FUT1 FUT2 FUT4 FUT8 G6PD GALC GALNT14 GALNT3 GAPDH GAPDHS GAS1 GBE1 GCNT2 GCNT3 GFRA1 GGT1 GLB1 GLO1 GLT8D1 GNS GOLPH3 GPAM GPAT2 GPC3 GPC6 GPLD1 GPNMB GPX1 GPX3 HADHB HAS2 HAS3 HK1 HMGCL HPGDS HPRT1 HPSE HS2ST1 HS3ST5 HSD11B1 HSD11B2 HSD17B12 HSPG2 HYAL2 ICAM1 IDH1 IDH2 IDUA IGF2R IL18R1 IL1RAPL1 INPP4B INPP5D INPP5E INPP5K ISYNA1 KL KLRB1 KLRC1 KLRK1 L1CAM LDHA LGALS1 LGALS3 LGALS9 LIPA LTA4H LYPD5 LYPLA1 LYPLA2 MAG MCAT MDH2 MELTF MGAT5 MGLL MICA MMP25 MOGS MPG MPPE1 MRC1 MTAP MUTYH NAMPT NCAM1 NEU1 NGLY1 NT5E OGG1 OS9 PARP1 PC PCK2 PCYT1A PDHB PDIA3 PFKFB2 PFKFB3 PFKFB4 PGK1 PIGU PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2A PKD1 PKM PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLAUR PLCB2 PLCB4 PLD1 PNP PNPLA2 PPARGC1A PPP1R3B PRKAA2 PRNP PSMD10 PTEN PTGDS PTGES PTGS1 PTGS2 PYGM RECK RPE RTN4R SCD5 SCD SDC1 SDC2 SDC4 SDHA SDHB SDHC SDHD SELE SELL SEMA7A SGMS1 SIGLEC1 SIGLEC7 SIGLEC9 SIRT2 SIRT6 SLC17A5 SLC2A2 SLC2A3 SLC33A1 SMPD1 SMUG1 SOAT1 SPAM1 ST3GAL4 ST6GALNAC2 ST8SIA1 STS SULF1 TKTL1 TLR4 TMED5 TNFRSF10C TP53 TPI1 UGT8 VCAM1 VCAN VTCN1	100507436 10082 1012 10135 10434 10457 10462 1048 10610 10682 10855 1087 10891 10956 11141 1116 11313 11343 120227 126129 128869 1374 142 1462 1464 150763 1545 1555 1571 1588 1589 1591 1594 1606 161198 1629 1636 1718 1942 202 2026 218 2181 2194 220 2215 2222 2224 222537 22914 22933 23213 2350 23583 23600 239 240 248 250 2523 2524 2526 2530 253782 2539 2581 2583 2591 259230 2597 2619 2632 26330 26503 2651 2674 2678 27036 27087 27180 2719 2720 27306 27349 2739 2799 2822 284348 2876 2878 2923 29956 3032 3037 3038 308 3098 310 3155 3251 3290 3291 3339 3383 3417 3418 3425 3482 353 3635 3820 3821 3897 3939 3956 3958 3965 3988 4048 4099 411 412 419 4191 4241 4249 427 43 4350 4360 4507 4595 4684 4758 48 4860 4907 4968 501 5091 50999 5106 51071 51144 51266 5130 51477 51548 5162 5167 51763 5208 5209 5210 5230 5289 5290 5291 5293 5294 5305 5310 5315 5319 5320 5321 5329 5330 5332 5337 54898 55331 5563 55768 55790 55830 55862 55907 5621 56623 57016 57104 57124 5716 5728 5730 5742 5743 57678 5837 6120 6319 6382 6383 6385 6389 6390 6391 6392 6401 6402 64083 64386 6484 6489 65078 6514 6515 65258 6609 6614 6646 6677 673 684 7099 7157 7167 7368 7412 7841 79623 79660 79679 79966 811 821 8277 8398 8416 8434 847 8482 8692 8794 8809 8821 9023 912 9162 9197 9245 929 933 9365 952 9536 960 9653 9695 972	Homo sapiens (human)
DOID:10811	nasal cavity cancer Aliases: malignant neoplasm of nasal cavities malignant tumor of the nasal cavity	TP53	7157	Homo sapiens (human)
DOID:1768	conversion disorder Aliases: Conversion Hysterical Neurosis Conversion hysteria or reaction Hysterical neurosis, conversion type	ABO ACHE COMT MMUT PIK3CA PRNP	1312 28 43 4594 5290 5621	Homo sapiens (human)
DOID:14686	Axenfeld-Rieger syndrome Aliases: Anomaly, Rieger's Axenfeld syndrome RGS - Rieger syndrome Rieger's anomaly	B3GLCT CRPPA CYP1B1 FKRP FKTN LARGE1 POMT1 POMT2 PTGDS	10585 145173 1545 2218 29954 5730 729920 79147 9215	Homo sapiens (human)
DOID:1143	exotropia Aliases: Divergent Strabismus Divergent concomitant strabismus	ACADSB DPAGT1 HADHA NGLY1 PIGQ PRPS1 SLC17A5 SLC35A2	1798 26503 3030 36 55768 5631 7355 9091	Homo sapiens (human)
DOID:9768	heart aneurysm Aliases: cardiac aneurysm	SMUG1	23583	Homo sapiens (human)
DOID:0070119	Meckel syndrome 5 Aliases: MKS5 Meckel-Gruber syndrome, type 5	ALG8 ALG9 ARF4 PKD1 PKD2 UMOD	378 5310 5311 7369 79053 79796	Homo sapiens (human)
DOID:0110724	neuronal ceroid lipofuscinosis 8 northern epilepsy variant Aliases: EPMR northern epilepsy variant, neuronal ceroid lipofuscinosis, Northern epilepsy variant progressive epilepsy with mental retardation, northern epilepsy progressive epilepsy-intellectual disability syndrome, Finnish type	ACLY ARSG CLN5 EPM2A GAD1 GAD2 LGALS1 PKD1 PPT1 PPT2 PSAP	1203 22901 2571 2572 3956 47 5310 5538 5660 7957 9374	Homo sapiens (human)
DOID:5246	obsolete hilar cholangiocellular carcinoma	HK1 PIK3CA PIK3CB PIK3CD PIK3CG PKM SDC2 SMUG1	23583 3098 5290 5291 5293 5294 5315 6383	Homo sapiens (human)
DOID:0110212	Charcot-Marie-Tooth disease X-linked recessive 4 Aliases: CMT4X CMTX4 Charcot-Marie-Tooth disease with deafness and mental retardation Cowchock syndrome NADMR NAMSD X-linked Charcot-Marie-Tooth disease type 4 axonal motor sensory neuropathy with deafness and mental retardation	ACE AMACR ARSA CANX CAT CD44 CYP4F3 DGAT2 FIG4 GBA1 GPX2 HADHB HK1 HPSE LCAT LPIN1 MAG MTM1 MTMR2 PGK1 PGM1 PLCB4 PLCE1 PRNP PRPS1 PTGS2 SIGLEC7 SPTLC1 SPTLC2	10558 10855 1636 23175 23600 2629 27036 2877 3032 3098 3931 4051 4099 410 4534 51196 5230 5236 5332 5621 5631 5743 821 84649 847 8898 9517 960 9896	Homo sapiens (human)
DOID:0060254	Robinow syndrome Aliases: Robinow dwarfism acral dysostosis with facial and genital abnormalities fetal face syndrome	ACADS AMT ARSA ARSD B4GALT7 BAAT CAT CHPT1 CYP11A1 DAG1 DCN DHDDS FOLR1 GALNT14 GAPDH GCSH GLB1 GLDC GPI HSPG2 KL OGG1 PARP1 PGAM2 PIK3CA PIK3CB PIK3CD PIK3CG PRNP PTEN SGPL1 SMC3 STS TNKS XYLT2	11285 142 1583 1605 1634 2348 2597 2653 2720 2731 275 2821 3339 35 410 412 414 4968 5224 5290 5291 5293 5294 5621 56994 570 5728 64132 79623 79947 847 8658 8879 9126 9365	Homo sapiens (human)
DOID:9351	diabetes mellitus Aliases: diabetes	ABO ACACA ACACB ACADSB ACAT1 ACE ACHE ACLY ACOT2 ACOT7 ACSL1 ACSM3 ACSS2 ADH1B ADH1C AGA AGPAT2 AKR1A1 AKR1B10 AKR1B1 AKR1C2 AKR1D1 ALDH2 ALDH6A1 ALDH7A1 ALDOB ALG1 ALOX12 ALOX5 ALPI ALPL ALPP AMACR AMY1A AMY1B AMY1C ANXA5 APRT ARSA ASAH2 ATP6AP2 ATRNL1 B4GALT5 BAAT C1GALT1 CA4 CALR CANX CAT CBR1 CBR3 CD14 CD1D CD33 CD38 CD44 CD48 CD55 CDH13 CEACAM5 CEACAM7 CEL CERS2 CERS6 CHAT CHGA CHI3L1 CHIT1 CHPT1 CHST3 CLEC16A CLEC1B COG2 COL9A2 COLEC12 COMT CPT1A CPT2 CS CTNS CYB5R4 CYP11A1 CYP11B2 CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP1B1 CYP21A2 CYP24A1 CYP27A1 CYP27B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP2E1 CYP2J2 CYP2R1 CYP3A4 CYP3A5 CYP46A1 CYP4A11 CYP4F3 CYP51A1 CYP7A1 CYP7B1 CYP8B1 DAG1 DCN DDOST DEGS1 DEGS2 DGAT1 DGCR2 DGKB DGKD DGKQ DGKZ DHCR7 DLAT DLD DSE DSEL EBP ELOVL3 ELOVL4 ELOVL5 ELOVL6 ENO1 ENO2 ENPP1 EPHX2 EXT1 EXT2 FADS1 FADS2 FASN FBP1 FCGR3B FCN3 FDPS FOLR2 FUCA1 FUT2 G6PC1 G6PC2 G6PD GAD1 GAD2 GAL3ST1 GALNS GALNT2 GALNT3 GAPDH GAPDHS GAS1 GBE1 GCK GFPT1 GFPT2 GGT1 GK GLA GLB1 GLO1 GLUL GNPDA2 GNPNAT1 GPAT4 GPC5 GPD1 GPD2 GPI GPIHBP1 GPX1 GPX3 GUSB GYG1 GYS1 H6PD HACD1 HADH HADHA HAS2 HAS3 HGSNAT HJV HK1 HK2 HMGCS2 HPGDS HPSE HS6ST1 HS6ST3 HSD11B1 HSD11B2 HSD17B12 HSD17B3 HSD17B6 HSD17B7 HSD3B1 HSPG2 ICAM1 IDH3A IDH3B IGF2R IL18R1 IL1R1 IMPA1 INPP5F INPPL1 INS ISYNA1 ITLN1 ITPK1 KCNJ11 KDSR KL KLB KLRK1 L1CAM LARGE1 LDHA LDHB LGALS1 LGALS2 LGALS3 LGALS4 LIPA LIPC LIPG LPIN1 LPIN2 LPL LY75 LYPLA1 LYZ MAN1A1 MAN2A1 MASP1 MASP2 MBL2 MBOAT7 MCAT MDH2 ME1 MGAM MGAT2 MGAT4A MGAT4C MGLL MICA MIOX MLYCD MMUT MOGAT2 MPG MPI MRC1 MSMO1 MTM1 MTMR3 MUTYH NAAA NAGLU NAMPT NANS NCAM1 NDST1 NEIL1 OGA OGG1 OGT OLR1 OXCT1 PAPSS2 PARP1 PARP2 PC PCK1 PCK2 PCYT1A PCYT1B PDHB PDHX PDX1 PEMT PFKFB2 PFKFB3 PFKM PGM1 PGP PHOSPHO1 PIK3C2A PIK3C2G PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1B PKD1 PKLR PLA2G10 PLA2G15 PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLA2G7 PLAUR PLB1 PLCB1 PLCB3 PLCD1 PLCG1 PLD1 PMM2 PNLIP PNPLA2 PNPLA3 PNPLA6 POMGNT1 PPP1R3A PPP1R3B PPP1R3C PRKAA2 PRSS21 PRSS8 PSMD10 PTEN PTGDS PTGES2 PTGIS PTGS1 PTGS2 PYGB REG1B RENBP RFT1 RPE RPN2 RTN4R RTN4RL1 SACM1L SCD5 SCD SDC1 SDC2 SDC4 SDHA SELE SELL SELP SFTPA1 SFTPC SFTPD SGMS1 SGSH SI SIGLEC1 SIGLEC5 SIGLEC7 SIRT2 SIRT4 SIRT6 SLC17A5 SLC2A10 SLC2A1 SLC2A2 SLC2A3 SLC2A4 SLC2A5 SLC33A1 SLC35A1 SLC35B3 SLC35G1 SLC37A4 SLC39A8 SLC3A1 SLC5A1 SMPD1 SMUG1 SOAT1 SORD SPHK1 SPHK2 SPTLC1 SRD5A1 SRD5A2 SRGN ST3GAL3 ST3GAL4 ST6GAL1 ST6GALNAC3 ST8SIA4 STS SUCLA2 SULF2 SULT1E1 TALDO1 THEM4 TKFC TKT TKTL1 TKTL2 TLR4 TM7SF2 TNKS2 TREH TYMP UGCG UGGT2 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UGT2B15 UMOD UPP1 UPP2 VCAM1 VTCN1 XYLT1 XYLT2	10038 100507436 1012 10135 10159 10327 10400 10434 1048 10555 10558 10559 1056 10682 10724 10747 10855 10858 1087 10908 10942 10965 1103 1113 1116 1118 11181 11320 11332 11343 117145 120227 123099 125 126 1298 1312 132789 1374 1376 137964 138050 142 1431 146760 148738 1497 151056 151531 152831 1543 1544 1545 1555 1557 1558 1559 1571 1573 1576 1577 1579 1581 1582 1583 1585 1586 1588 1589 1591 1593 159371 1594 1595 1604 1605 1607 1609 162466 1634 1636 1646 1650 1717 1737 1738 175 1890 2023 2026 2053 2131 2132 217 2180 2194 2203 2215 2224 2262 22796 22876 229 22908 22914 22933 231 23175 23236 23274 23409 23417 2350 23583 23600 23659 239 240 248 249 250 2517 2524 2531 253782 2538 2539 2542 256435 2571 2572 25834 2588 2590 2591 259230 2597 26007 26033 2619 2632 26330 2645 26503 266722 2673 2678 27036 2710 27163 2717 2720 27306 27349 2739 2752 276 277 278 28 2819 2820 2821 283871 2876 2878 2990 2992 29940 29956 2997 3030 3033 3037 3038 308 3098 3099 31 3158 32 3283 3290 3291 3293 3339 3340 3383 338328 3419 3420 3482 353 3554 36 3612 3630 3636 3651 3705 3767 38 3897 3939 3945 3956 3957 3958 3960 3988 3990 3992 4023 4051 4065 4069 410 412 4121 4124 4153 4191 4199 4247 43 4329 4350 4351 4360 4534 4594 4595 4669 4684 47 4968 4973 501 5019 5091 51000 5105 5106 51144 51167 51266 5130 51477 51478 51548 5162 5167 5208 5209 5213 5236 5286 5288 5289 5290 5291 5293 5294 5310 5313 5319 5320 5321 5329 5331 5333 5335 5337 5373 5406 54187 54575 54576 54577 54578 54579 54600 54657 54658 54659 5506 5507 5552 55586 55600 55624 5563 55757 55902 55959 56052 5648 5652 56624 56848 56913 56994 570 57016 57104 5716 5728 5730 5740 5742 5743 57818 5834 5968 5973 60481 6120 6185 6296 6307 6319 6382 6383 6385 6389 6401 6402 6403 64116 64131 64132 6440 6441 6448 6476 6480 6484 64841 6487 65078 6513 6514 6515 6517 6518 6519 6523 653509 6609 6614 6646 6652 6715 6716 6718 6783 6785 6888 7086 7099 7108 7357 7366 7369 7378 7412 762 7903 79071 79143 7941 79660 79661 79679 79966 80142 80168 80339 80351 8050 81031 81035 811 821 8277 83401 8395 8398 8399 84076 847 8473 8525 8527 8547 8560 8630 8694 873 874 8778 8803 8809 8877 8897 8972 9060 912 91869 9197 9200 92126 9215 929 9334 9365 9388 9394 9415 9420 945 9468 9469 9514 952 9563 960 962 9663 9945 9993	Homo sapiens (human)
DOID:4948	gallbladder carcinoma Aliases: cancer of the gallbladder carcinoma gallbladder carcinoma of gallbladder	ABO ACE ALDH1A3 ANXA5 APRT CAT CD44 CEACAM5 CEACAM6 CEACAM7 CNTN4 CYP17A1 CYP1A1 CYP1B1 CYP27A1 CYP2B6 CYP39A1 CYP7A1 CYP7B1 FKTN GALNT3 GCNT2 GGT1 GPC1 GPC3 GPX3 HK2 HPGDS HPSE HSD17B7 HSPG2 IDH1 ISYNA1 LDHA MPG NT5E OGG1 PC PGK1 PIK3CA PIK3CB PIK3CD PIK3CG PKLR PKM PLCE1 PSAP PTEN PTGS2 SDC1 SDC2 SMUG1 SPHK1 ST8SIA4 SULT2B1 TYMP	1048 10855 1087 152330 1543 1545 1555 1581 1586 1593 1636 1890 220 2218 23583 2591 2651 2678 2719 27306 28 2817 2878 308 3099 3339 3417 353 3939 4350 4680 4907 4968 5091 51196 51302 51477 51478 5230 5290 5291 5293 5294 5313 5315 5660 5728 5743 6382 6383 6820 7903 847 8877 9420 960	Homo sapiens (human)
DOID:4031	eosinophilic gastroenteritis	SIGLEC8	27181	Homo sapiens (human)
DOID:9503	Loeffler syndrome Aliases: Loeffler's pneumonia Loffler's syndrome	ALPL CEL CHI3L1 HPGDS IL1R1 IL1RL1 ISYNA1 PARP9 PTGDS SIGLEC8 SIRT2 SLC27A5	1056 10998 1116 22933 249 27181 27306 3554 51477 5730 83666 9173	Homo sapiens (human)
DOID:0110459	dilated cardiomyopathy 1FF Aliases: CMD1FF	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)
DOID:0050456	Buruli ulcer disease Aliases: Bairnsdale ulcer Daintree ulcer Mossman ulcer Searl ulcer Searle's ulcer	LTA4H	4048	Homo sapiens (human)
DOID:0110511	autosomal recessive nonsyndromic deafness 59 Aliases: DFNB59 autosomal recessive deafness 59	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)
DOID:0080159	Cryptococcal meningitis	CYP51A1 MBL2	1595 4153	Homo sapiens (human)
DOID:7165	subacute thyroiditis Aliases: De Quervain's thyroiditis Giant-cell thyroiditis Granulomatous thyroiditis Subacute Granulomatous Thyroiditis	GUSB SMUG1	23583 2990	Homo sapiens (human)
DOID:0070134	autosomal recessive cutis laxa type IIA Aliases: ARCL2A	ATP6AP1 ATP6V0A2 ATP6V1A B3GALT6 B3GAT3 B4GALT7 CAT CHST3 DCN DHCR7 ECHS1 ENOSF1 MAN1B1 PARP1 PIGL PLCG2 PMM2 PTDSS1 SLC2A10 SRD5A3	11253 11285 126792 142 1634 1717 1892 23545 26229 523 5336 537 5373 55556 79644 81031 847 9469 9487 9791	Homo sapiens (human)
DOID:4648	familial retinoblastoma Aliases: Hereditary Retinoblastoma	APRT CBR3 CD44 CDH13 CEACAM5 CEACAM7 CEMIP EBP EFNA2 ENO1 ENO2 FASN FOLR1 FUT7 GLB1 GPC6 GPI HPGDS ICAM1 IDH1 IDH2 IGF2R KLRK1 L1CAM LDHA LGALS3 LIPG MICA MMUT MPG MTAP NCAM1 PGP PIGF PIK3CA PIK3CB PIK3CD PIK3CG PNPLA2 PSMD10 PTEN PTGES3 PTGS2 RENBP RPE SIGLEC7 SOAT1 SUCLA2 TIGAR ULBP2	100507436 10082 1012 1048 10682 10728 1087 1943 2023 2026 2194 22914 2348 2529 27036 2720 27306 2821 283871 3383 3417 3418 3482 353 3897 3939 3958 4350 4507 4594 4684 5281 5290 5291 5293 5294 57103 57104 5716 57214 5728 5743 5973 6120 6646 80328 874 8803 9388 960	Homo sapiens (human)
DOID:0060222	Scheie syndrome Aliases: mucopolysaccharidosis type 1S mucopolysaccharidosis type IS mucopolysaccharidosis type V	ARSB CAT FUT1 IDUA	2523 3425 411 847	Homo sapiens (human)
DOID:0050557	congenital muscular dystrophy	ACE ACHE AGK AGL APRT B3GALNT2 B4GALNT2 B4GAT1 CHKA CHKB COL6A1 CRPPA DAG1 DCN DPEP1 DPM1 DPM2 DPM3 ENO1 FKRP FKTN GK GLB1 GMPPB HPGDS IDH2 IMPA1 INPP5B INPP5K LARGE1 LARGE2 LGALS3 MBL2 MGAM PARP1 PIK3C2A PMM2 POGLUT1 POMGNT1 POMGNT2 POMK POMT1 POMT2 PRG2 RXYLT1 SDC2 SI SYNJ1 SYNJ2	10329 10585 11041 1119 1120 120071 124872 1291 142 148789 1605 1634 1636 178 1800 2023 2218 2710 2720 27306 29925 29954 3418 353 3612 3633 3958 4153 43 51763 5286 5373 54344 5553 55624 55750 56983 6383 6476 729920 79147 84197 84892 8813 8818 8867 8871 8972 9215	Homo sapiens (human)
DOID:0060326	myelomeningocele	ABO ACHE ARSA CD38 CHKA COMT FOLR1 FOLR2 GPC5 HK1 ISYNA1 ITPK1 PCYT1A SLC2A1 SLC2A2 SLC2A3 UGCG	1119 1312 2262 2348 2350 28 3098 3705 410 43 5130 51477 6513 6514 6515 7357 952	Homo sapiens (human)

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