GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	January 28, 2025
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **1026 - 1050** of **4115** in total

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Disease ID	Disease Name ▼	Gene Symbol	Gene ID	Organism	Source
DOID:0080096	myofibrillar myopathy 5 Aliases: filaminopathy	FLNC	2318	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080095	myofibrillar myopathy 4 Aliases: zaspopathy	LDB3	11155	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080093	myofibrillar myopathy 2 Aliases: alpha-b crystallinopathy	CRYAB	1410	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112108	myofibrillar myopathy 10 Aliases: MFM10	SVIL	6840	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080092	myofibrillar myopathy 1 Aliases: autosomal recessive limb-girdle muscular dystrophy type 2R desminopathy	DES	1674	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060475	myoclonic-atonic epilepsy Aliases: EEOC childhood onset epileptic encephalopathy	SLC6A1	6529	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090034	myoclonic dystonia 11	SGCE	8910	Homo sapiens (human)	Alliance of Genome Resources
DOID:820	myocarditis Aliases: Myocardial inflammation	HLA-DQB1	3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:5844	myocardial infarction Aliases: Myocardial infarct heart attack	ACE ADD1 ADRB2 AGER AGT AGTR1 ALDH2 ANXA5 APEX1 APOA1 APOA4 APOE APOH BRINP3 CCL2 CCR2 CD14 CIITA CLU COL4A1 COL6A3 CSF3 CTLA4 CYP2J2 CYP2R1 EPO ESR1 F12 F13A1 F2 F5 F7 FGB FTO GCLC GP1BA GP6 HFE HGF HIF1A HP IL10 IL18BP ITGA2 ITGB3 ITIH4 KCNN4 KDR KLK1 LGALS2 LIPG LPA LPL LRP1 LRP8 LRPAP1 LTA MLXIPL MMP14 MMP1 MMP3 MMP9 NGF NOS3 NPPA NPPB NPR1 NR1H3 NRG1 OLR1 PAPPA PCSK2 PECAM1 PGF PLAT PLAU PON1 PPARA PSMA6 PTGIS PTGS2 SELP SERPINE1 SOD1 SOD3 SPP1 TFPI TGFB1 TLR4 TNFSF4 VEGFB	10062 10068 118 1191 120227 1282 1293 1440 1493 154 1573 1636 177 183 185 2056 2099 2147 2153 2155 2161 2162 217 2244 2729 2811 3077 308 3082 3084 3091 3240 328 335 337 339479 348 350 3586 3673 3690 3700 3783 3791 3816 3957 4018 4023 4035 4043 4049 4261 4312 4314 4318 4323 4803 4846 4878 4879 4881 4973 5054 5069 51085 51206 5126 5175 5228 5327 5328 5444 5465 5687 5740 5743 6347 6403 6647 6649 6696 7035 7040 7099 7292 729230 7423 7804 79068 929 9388	Homo sapiens (human)	Alliance of Genome Resources
DOID:2226	myeloproliferative neoplasm Aliases: CMPD CMPD, U chronic myeloproliferative disease	PDGFRB TET2	5159 54790	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111344	myeloproliferative disorder with eosinophilia Aliases: chronic myeloproliferative disorder with eosinophilia	PDGFRB	5159	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060326	myelomeningocele	SLC2A1	6513	Homo sapiens (human)	Alliance of Genome Resources
DOID:8683	myeloid sarcoma Aliases: Chloroma Extramedullary Myeloid tumor Granulocytic sarcoma	KRAS PDGFRA	3845 5156	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070004	myeloid neoplasm	CBL FGFR1 GPX1 MECOM	2122 2260 2876 867	Homo sapiens (human)	Alliance of Genome Resources
DOID:8692	myeloid leukemia Aliases: Non-Lymphocytic Leukemia leukaemia myelogenous leukemia myelogenous myeloid granulocytic leukaemia myeloid granulocytic leukemia myeloid leukaemia	FGFR1 GATA2 IFNG MN1 NSD3 PDGFRA UGT1A1	2260 2624 3458 4330 5156 54658 54904	Homo sapiens (human)	Alliance of Genome Resources
DOID:4971	myelofibrosis Aliases: Agnogenic myeloid metaplasia Aleukemic myelosis Megakaryocytic myelosclerosis bone Marrow Fibrosis myelosclerosis primary myelofibrosis	ASXL1 CALR EZH2 HFE KMT2A MPL	171023 2146 3077 4297 4352 811	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050908	myelodysplastic syndrome	ARPC1B ASXL1 CDKN1B CSF3R EZH2 FCGR3A GATA2 GNB1 HFE IDH1 MEFV NRAS PLCB1 SF3B1 SRSF2 TET2 TP53 XRCC1 ZRSR2	10095 1027 1441 171023 2146 2214 23236 23451 2624 2782 3077 3417 4210 4893 54790 6427 7157 7515 8233	Homo sapiens (human)	Alliance of Genome Resources
DOID:322	myelitis	HLA-DPB1	3115	Homo sapiens (human)	Alliance of Genome Resources
DOID:8691	mycosis fungoides Aliases: mycosis fungoides lymphoma	HLA-DQB1	3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:437	myasthenia gravis	ACHE ADRB2 CHRM1 HLA-DQA1 HLA-DQB1 HLA-DRB1 IL2RB	1128 154 3117 3119 3123 3560 43	Homo sapiens (human)	Alliance of Genome Resources
DOID:4189	mutism	CNTNAP2	26047	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112374	muscular dystrophy-dystroglycanopathy Aliases: MDDG	GMPPB	29925	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112382	muscular dystrophy-dystroglycanopathy type C8 Aliases: LGMDR24 MDDGC2 autosomal recessive limb-girdle muscular dystrophy 24 muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 8 muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT2-related	POMGNT2	84892	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112381	muscular dystrophy-dystroglycanopathy type C12 Aliases: LGMD due to POMK deficiency Limb-girdle muscular dystrophy due to POMK deficiency MDDGC12 muscular dystrophy-dystroglycanopathy, limb-girdle, POMK-related	POMK	84197	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110637	muscular dystrophy-dystroglycanopathy type B6 Aliases: MDC1D MDDGB6 congenital muscular dystrophy LARGE-related congenital muscular dystrophy type 1D muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6 muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6	LARGE1	9215	Homo sapiens (human)	Glyco-Disease Genes Database Alliance of Genome Resources

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