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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **876 - 900** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
401494	3-hydroxyacyl-CoA dehydratase 4	HACD4 Aliases: Em:AL662879.1 OTTHUMG00000021016 Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4	Homo sapiens (human)	arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer
51495	3-hydroxyacyl-CoA dehydratase 3	HACD3 Aliases: B-ind1 HSPC121 Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 3	Homo sapiens (human)	depressive disorder dysthymic disorder major depressive disorder melancholic depression neurotic disorder obsolete melancholia
201562	3-hydroxyacyl-CoA dehydratase 2	HACD2 Aliases: Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2	Homo sapiens (human)	cancer
9200	3-hydroxyacyl-CoA dehydratase 1	HACD1 Aliases: CAP Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1 cementum attachment protein	Homo sapiens (human)	B-cell lymphoma Ehrlich tumor carcinoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Laron syndrome Lyme disease Perry syndrome Streptococcus pneumonia T-cell acute lymphoblastic leukemia X-linked dilated cardiomyopathy achondroplasia acute biphenotypic leukemia acute leukemia agnosia allergic asthma allergic rhinitis androgen insensitivity syndrome anthrax disease aplastic anemia arrhythmogenic right ventricular cardiomyopathy asthma autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy beta thalassemia bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma cancer centronuclear myopathy cerebral infarction cerebrovascular disease cervix uteri carcinoma in situ childhood osteosarcoma clubfoot colitis common cold congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congenital myopathy 4A congenital myopathy congenital ptosis congenital structural myopathy cryptococcosis cryptorchidism developmental coordination disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal myopathy embryoma epilepsy facioscapulohumeral muscular dystrophy gastroenteritis giant cell glioblastoma glioblastoma hepatitis B hepatitis C hepatocellular carcinoma high grade glioma ileitis ileocolitis influenza intellectual disability intrinsic asthma learning disability limb-girdle muscular dystrophy liver cancer liver cirrhosis mantle cell lymphoma megaconial type congenital muscular dystrophy multidrug-resistant tuberculosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy nemaline myopathy obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete ymphosarcoma oculopharyngeal muscular dystrophy ophthalmoplegia osteosarcoma ovarian cancer ovarian carcinoma paroxysmal nocturnal hemoglobinuria pleural empyema pneumonia polycystic ovary syndrome polyhydramnios premature menopause primary ovarian insufficiency prostate cancer prostate carcinoma ptosis recurrent hypersomnia rigid spine muscular dystrophy 1 scoliosis sick sinus syndrome steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder thalassemia thymic carcinoma thymoma tuberculosis type 2 diabetes mellitus type C thymoma vasomotor rhinitis viral infectious disease wheat allergy
22927	hyaluronan binding protein 4	HABP4 Aliases: IHABP4 SERBP1L	Homo sapiens (human)	Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma
9563	hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase	H6PD Aliases: 6-phosphogluconolactonase GDH/6PGL endoplasmic bifunctional protein H6PDH	Homo sapiens (human)	Alzheimer's disease B-cell lymphoma Laron syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis beta thalassemia breast cancer breast carcinoma cancer cardiovascular system disease cholangiocarcinoma colorectal cancer cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease cortisone reductase deficiency 1 cortisone reductase deficiency dementia diabetes insipidus diabetes mellitus diabetic ketoacidosis diarrhea gallbladder disease giardiasis heart disease hemolytic anemia hyperandrogenism hyperinsulinism hypertrichosis hypoglycemia infertility intrahepatic cholangiocarcinoma large intestine cancer leishmaniasis liver disease luminal breast carcinoma A malaria multiple sclerosis neurohypophyseal diabetes insipidus obesity obsolete ymphosarcoma placental insufficiency polycystic ovary syndrome primary hyperoxaluria steatotic liver disease thalassemia type 2 diabetes mellitus visceral leishmaniasis
2998	glycogen synthase 2	GYS2	Homo sapiens (human)	Baraitser-Winter syndrome Fraser syndrome Gerstmann-Straussler-Scheinker syndrome Goldenhar syndrome Gorham's disease Joubert syndrome 1 Joubert syndrome Lafora disease Laron syndrome Moebius syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia adult medulloblastoma branchiootic syndrome cancer childhood medulloblastoma cystinuria disease of metabolism epilepsy familial hyperlipidemia galactosemia gestational diabetes glucosephosphate dehydrogenase deficiency glycogen storage disease III glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis B hepatocellular carcinoma hyperglycemia hypoglycemia liver cancer medulloblastoma medullomyoblastoma melanotic medulloblastoma orofaciodigital syndrome I orofaciodigital syndrome X orofaciodigital syndrome polycystic ovary syndrome visual epilepsy
2997	glycogen synthase 1	GYS1 Aliases: GSY	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lafora disease abdominal obesity-metabolic syndrome 1 acute myocardial infarction arthritis arthropathy cardiomyopathy cardiovascular system disease coronary thrombosis diabetes mellitus diabetic ketoacidosis endomyocardial fibrosis essential thrombocythemia hypertrophic cardiomyopathy hypoglycemia myelodysplastic syndrome myocardial infarction obsolete type 1 diabetes mellitus 9 rheumatoid arthritis silent myocardial infarction type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus visual epilepsy
8908	glycogenin 2	GYG2 Aliases: GN-2 glycogenin glucosyltransferase	Homo sapiens (human)	Leigh disease cystinuria galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease
2992	glycogenin 1	GYG1 Aliases: glycogenin glucosyltransferase	Homo sapiens (human)	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Lafora disease cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia central nervous system origin vertigo coronary artery disease cystinuria diabetes mellitus disease of metabolism endomyocardial fibrosis familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease XV glycogen storage disease hypertrophic cardiomyopathy myopathy sick sinus syndrome type 2 diabetes mellitus
727936	glucoside xylosyltransferase 2	GXYLT2	Homo sapiens (human)
283464	glucoside xylosyltransferase 1	GXYLT1 Aliases: FLJ43151	Homo sapiens (human)
2990	glucuronidase beta	GUSB	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Clouston syndrome Crohn's colitis Crohn's disease De Quervain disease Fabry disease Laron syndrome Pick's disease Reye syndrome Richter's syndrome Sly syndrome Werner syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adenosarcoma adrenal gland cancer alcohol dependence alcohol use disorder alternating hemiplegia of childhood arteriosclerotic cardiovascular disease arteriovenous malformation arthritis arthropathy atherosclerosis autonomic neuropathy bladder carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system disease cerebral degeneration cholecystolithiasis choledocholithiasis cholelithiasis chondrodysplasia punctata chronic lymphocytic leukemia chronic myeloid leukemia chylomicron retention disease clubfoot colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease cystic fibrosis diabetes mellitus diabetic ketoacidosis diarrhea duodenum cancer elephantiasis embryoma endomyocardial fibrosis factor VIII deficiency familial adenomatous polyposis 1 familial adenomatous polyposis follicular adenoma gallbladder disease gastroenteritis gastrointestinal system disease gingival hypertrophy gingival overgrowth glycoproteinosis head and neck cancer head and neck squamous cell carcinoma heart cancer hepatitis B hepatitis C hepatitis hepatocellular carcinoma herpes simplex hydrocephalus hyperglycemia hypertrichosis hypertrophic cardiomyopathy ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intestinal disease islet cell tumor large intestine cancer learning disability lipid storage disease liver cancer liver disease lung adenocarcinoma lung cancer lung carcinoma lymphedema lysosomal storage disease microcystic adenoma mucolipidosis II alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myeloproliferative neoplasm nasopharynx carcinoma nephroblastoma nervous system disease neuroblastoma neurodegenerative disease obstructive hydrocephalus omphalocele ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma paraganglioma peritonitis pheochromocytoma progeria prostate cancer prostate carcinoma proteinuria pulmonary tuberculosis recurrent corneal erosion retinal disease retinitis rheumatoid arthritis sarcomatoid carcinoma schizophrenia scoliosis senile degeneration of brain sensorineural hearing loss shigellosis small intestine cancer stomach cancer stomach carcinoma subacute thyroiditis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis umbilical hernia urinary bladder cancer
79712	glycosyltransferase like domain containing 1	GTDC1 Aliases: FLJ11753 Hmat-Xa mannosyltransferase-like	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome aphthous stomatitis cerebral degeneration schizophrenia
119391	glutathione S-transferase omega 2	GSTO2	Homo sapiens (human)	Alzheimer's disease Parkinson's disease alcohol use disorder asthma
9446	glutathione S-transferase omega 1	GSTO1	Homo sapiens (human)	Alzheimer's disease Parkinson's disease alcohol use disorder
2932	glycogen synthase kinase 3 beta	GSK3B	Homo sapiens (human)	Alzheimer's disease Parkinson's disease acute myocardial infarction amyotrophic lateral sclerosis bipolar disorder colon cancer colorectal adenocarcinoma degenerative disc disease depressive disorder diabetic encephalopathy endometrial carcinoma heart disease hypertension middle cerebral artery infarction myocardial infarction oral squamous cell carcinoma schizophrenia sciatic neuropathy status epilepticus substance-related disorder type 2 diabetes mellitus vascular dementia
2931	glycogen synthase kinase 3 alpha	GSK3A	Homo sapiens (human)	Parkinsonism amyotrophic lateral sclerosis
402635	galectin-related inter-fiber protein	GRIFIN	Homo sapiens (human)
9380	glyoxylate and hydroxypyruvate reductase	GRHPR Aliases: PH2 primary hyperoxaluria type 2	Homo sapiens (human)	atypical hemolytic-uremic syndrome calcinosis calcium metabolism disease chronic kidney disease hemolytic-uremic syndrome hypercalcemia kidney failure nephrocalcinosis nephrolithiasis phosphorus metabolism disease primary hyperoxaluria type 2 primary hyperoxaluria prostate cancer prostate carcinoma ureteral obstruction uric acid nephrolithiasis urinary tract obstruction
493869	glutathione peroxidase 8 (putative)	GPX8 Aliases: EPLA847 UNQ847	Homo sapiens (human)
2882	glutathione peroxidase 7	GPX7 Aliases: FLJ14777 GPX6 NPGPx	Homo sapiens (human)	Barrett's adenocarcinoma Barrett's esophagus Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease amyotrophic lateral sclerosis breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma cancer embryoma esophagus adenocarcinoma hyperhomocysteinemia lung cancer progressive muscular atrophy
257202	glutathione peroxidase 6	GPX6 Aliases: selenoprotein GPX6	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease breast cancer depressive disorder lung squamous cell carcinoma major depressive disorder melancholic depression obsolete melancholia ovarian cancer ovarian carcinoma
2880	glutathione peroxidase 5	GPX5 Aliases: epididymal androgen-related protein	Homo sapiens (human)	hyperglycemia
2878	glutathione peroxidase 3	GPX3 Aliases: selenoprotein GPX3	Homo sapiens (human)	Barrett's adenocarcinoma Barrett's esophagus Down syndrome Duchenne muscular dystrophy Fanconi syndrome Kuhnt-Junius degeneration Sveinsson chorioretinal atrophy abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute kidney failure acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma age related macular degeneration agnosia allergic asthma amyotrophic lateral sclerosis androgen insensitivity syndrome arteriosclerotic cardiovascular disease asthma atherosclerosis autoimmune thyroiditis bacterial sepsis bipolar disorder breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma chronic kidney disease chronic myeloid leukemia chronic obstructive pulmonary disease clear cell adenocarcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal adenoma colorectal cancer colorectal carcinoma congenital heart disease coronary artery disease coronary thrombosis cribriform carcinoma cystinosis degeneration of macula and posterior pole depressive disorder diabetes mellitus diabetic ketoacidosis differentiated thyroid gland carcinoma dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism embryoma endometrial adenocarcinoma endometriosis of ovary endometriosis of uterus endometriosis endomyocardial fibrosis esophageal cancer esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia gallbladder cancer gallbladder carcinoma generalized atherosclerosis giant cell glioblastoma glioblastoma glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypertension hypertrophic cardiomyopathy inflammatory breast carcinoma intracranial sinus thrombosis intrinsic asthma invasive ductal carcinoma kidney disease kwashiorkor large intestine cancer leukemia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lymphoplasmacytic lymphoma macular degeneration male infertility marasmus melanoma mild pre-eclampsia multiple myeloma muscular dystrophy myelodysplastic syndrome myocardial infarction nasal type extranodal NK/T-cell lymphoma nephritis nephrosis nephrotic syndrome neurodegenerative disease nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete type 1 diabetes mellitus 9 ovarian cancer ovarian carcinoma papillary adenocarcinoma papillary renal cell carcinoma phenylketonuria poikiloderma with neutropenia polycystic ovary syndrome pre-eclampsia progressive muscular atrophy propionic acidemia prostate cancer prostate carcinoma protein-energy malnutrition pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinitis pigmentosa 30 sarcomatoid carcinoma sarcomatoid renal cell carcinoma sciatic neuropathy serous cystadenocarcinoma severe pre-eclampsia silent myocardial infarction skin melanoma spermatic cord torsion spondyloepimetaphyseal dysplasia, Sponastrime type stomach cancer stomach carcinoma systemic scleroderma thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma transient cerebral ischemia tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus vertebrobasilar insufficiency vitamin B12 deficiency

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