GlyCosmos Portal

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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 **151 - 175** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
23333	dpy-19 like C-mannosyltransferase 1	DPY19L1 Aliases: KIAA0877	Homo sapiens (human)
2720	galactosidase beta 1	GLB1 Aliases: EBP elastin binding protein	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 B-cell lymphoma Balo concentric sclerosis Behcet's disease Burkitt lymphoma Clostridium difficile colitis Cockayne syndrome Cornelia de Lange syndrome Costello syndrome Crohn's colitis Crohn's disease Dubowitz syndrome Duchenne muscular dystrophy Fabry disease GM1 gangliosidosis type 1 GM1 gangliosidosis type 2 GM1 gangliosidosis type 3 GM1 gangliosidosis GM2 gangliosidosis Gaucher's disease Kawasaki disease Krabbe disease Laron syndrome Niemann-Pick disease Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prader-Willi syndrome Reye syndrome Richter's syndrome Robinow syndrome Sandhoff disease Seckel syndrome Silver-Russell syndrome Silverman-Handmaker type dyssegmental dysplasia X-linked Aarskog syndrome X-linked dilated cardiomyopathy X-linked ichthyosis X-linked spondyloepiphyseal dysplasia tarda Zollinger-Ellison syndrome achondroplasia acquired immunodeficiency syndrome acute promyelocytic leukemia adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma adrenoleukodystrophy adult fibrosarcoma adult lymphoma allergic asthma anaplastic astrocytoma anogenital venereal wart aortic valve disease 2 aortic valve stenosis arthritis arthropathy aspartylglucosaminuria asthma atopic dermatitis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 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 Robinow syndrome 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 benign mesothelioma bladder carcinoma bladder urothelial carcinoma bone disease brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma bullous pemphigoid cancer carcinoma cardiomyopathy cartilage disease celiac disease central nervous system cancer central nervous system disease central nervous system lymphoma cerebellar ataxia cerebellar disease cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma childhood astrocytic tumor childhood cerebral astrocytoma childhood leukemia childhood lymphoma cholera chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma chronic kidney disease chronic lymphocytic leukemia chronic obstructive pulmonary disease chylomicron retention disease collagen disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital muscular dystrophy congestive heart failure connective tissue disease contact dermatitis corneal neovascularization cutaneous fibrous histiocytoma cystic fibrosis dental caries dentin caries depressive disorder dermatitis diabetes insipidus diabetes mellitus diabetic ketoacidosis diarrhea 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 dysostosis dystonia embryoma endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familial hypercholesterolemia familial hyperlipidemia familial hypertrophic cardiomyopathy familial retinoblastoma fibrillary astrocytoma fibrosarcoma filariasis focal hand dystonia fucosidosis galactosialidosis gangliosidosis gemistocytic astrocytoma generalized dystonia giant cell glioblastoma giant cell reparative granuloma gingival hypertrophy gingival overgrowth glioblastoma gliosarcoma glycoproteinosis head and neck cancer head and neck squamous cell carcinoma hepatitis B hepatoblastoma hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies herpes simplex hidradenoma high grade glioma human immunodeficiency virus infectious disease hydrocephalus hyperinsulinism hypertrichosis hypertrophic cardiomyopathy hypotrichosis 7 hypotrichosis idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia inherited metabolic disorder intellectual disability intracranial hypertension intrinsic asthma irritable bowel syndrome islet cell tumor juvenile pilocytic astrocytoma kwashiorkor lactose intolerance large intestine cancer learning disability leiomyoma leukemia limb-girdle muscular dystrophy lipid storage disease liver cancer liver cirrhosis localized scleroderma locked-in syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung large cell carcinoma lung small cell carcinoma lymphoma lysosomal storage disease major depressive disorder malignant astrocytoma malignant mesothelioma marasmus measles melancholic depression melanoma metachromatic leukodystrophy microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II mixed glioma mucolipidosis III alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia multiple myeloma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myofibroma narcolepsy nervous system disease neuroblastoma neurocirculatory asthenia neurodegeneration with brain iron accumulation neurodegenerative disease neurohypophyseal diabetes insipidus nevoid basal cell carcinoma syndrome nutrition disease obesity 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 melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma occupational dermatitis oculopharyngeal muscular dystrophy optic atrophy osteoarthritis osteochondrodysplasia osteoporosis ovarian cancer ovarian carcinoma pancytopenia papilloma parasitic helminthiasis infectious disease patent ductus arteriosus pilocytic astrocytoma postinflammatory pulmonary fibrosis primary biliary cholangitis primary immunodeficiency disease primary open angle glaucoma primary pulmonary hypertension progressive pseudorheumatoid arthropathy of childhood prostate cancer prostate carcinoma protein-energy malnutrition protoplasmic astrocytoma pseudotumor cerebri pulmonary fibrosis quadriplegia recurrent corneal erosion retinoblastoma rhabdomyosarcoma rheumatoid arthritis rippling muscle disease 2 sarcomatoid carcinoma scleroderma scoliosis sea-blue histiocytosis secondary Parkinson disease sensorineural hearing loss skin melanoma skin papilloma skin squamous cell carcinoma skin tag sphingolipidosis spondyloepiphyseal dysplasia congenita squamous cell papilloma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma synovial sarcoma syringoma systemic scleroderma tarsal-carpal coalition syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma transthyretin amyloidosis trilateral retinoblastoma 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 ulcerative colitis urinary bladder cancer uterine fibroid viral infectious disease visual epilepsy
3998	lectin, mannose binding 1	LMAN1 Aliases: ERGIC-53 ERGIC53 FMFD1 MCFD1 MR60 endoplasmic reticulum-golgi intermediate compartment protein 53 gp58	Homo sapiens (human)	IgA glomerulonephritis adenocarcinoma adenoma allergic disease arteriosclerotic cardiovascular disease atherosclerosis blood coagulation disease cancer carcinoma colorectal cancer congenital afibrinogenemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia coronary artery disease factor V deficiency factor VII deficiency factor VIII deficiency factor XIII deficiency follicular adenoma hematopoietic system disease large intestine cancer malaria microcystic adenoma nutmeg liver obsolete inherited blood coagulation disease papillary adenoma sarcomatoid carcinoma thanatophoric dysplasia vitamin K deficiency bleeding
4153	mannose binding lectin 2	MBL2	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 B-cell adult acute lymphocytic leukemia Balo concentric sclerosis Bannayan-Riley-Ruvalcaba syndrome Behcet's disease Burkitt lymphoma Chagas disease Clostridium difficile colitis Coronavirus infectious disease Cowden syndrome Crohn's colitis Crohn's disease Cryptococcal meningitis Duchenne muscular dystrophy Evans' syndrome Graves' disease Guillain-Barre syndrome HELLP syndrome Henoch-Schoenlein purpura Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Japanese encephalitis Kartagener syndrome Kawasaki disease Klebsiella pneumonia Legionnaires' disease Lyme disease Miller Fisher syndrome Pick's disease Plasmodium falciparum malaria Reye syndrome Richter's syndrome Sjogren's syndrome Streptococcus pneumonia Turner syndrome West Nile fever acquired immunodeficiency syndrome acrodermatitis acute interstitial pneumonia acute lymphoblastic leukemia acute myocardial infarction acute pancreatitis acute pericementitis acute poststreptococcal glomerulonephritis acute pyelonephritis adrenoleukodystrophy adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome age related macular degeneration aggressive periodontitis agranulocytosis allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis amyloidosis anal carcinoma in situ anemia angioedema ankylosing spondylitis anodontia anogenital venereal wart anthracosilicosis anthracosis antiphospholipid syndrome antithrombin III deficiency aortic valve insufficiency arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis aspergillosis asthma atherosclerosis atopic dermatitis autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autoimmune thyroiditis autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 bacterial infectious disease bacterial meningitis bacterial pneumonia bacterial sepsis bacterial vaginosis bipolar disorder black piedra bone inflammation disease brain ischemia breast cancer breast carcinoma bronchiectasis bronchiolitis obliterans bronchiolitis bronchitis bronchopneumonia bronchopulmonary dysplasia bronchus cancer bronchus carcinoma cancer candidiasis cardiac arrest cardiomyopathy cardiovascular system disease carotid artery disease cataract 32 multiple types celiac disease central nervous system cancer central nervous system disease central nervous system lymphoma cerebral degeneration cerebral infarction cerebral malaria cerebral palsy cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood B-cell acute lymphoblastic leukemia childhood type dermatomyositis chorioamnionitis chromosome 10q23 deletion syndrome chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia chronic obstructive pulmonary disease coccidioidomycosis colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common cold common variable immunodeficiency common wart complement component 2 deficiency congenital hypothyroidism congenital muscular dystrophy conjunctivitis coronary aneurysm coronary artery disease coronary restenosis coronary thrombosis cryptosporidiosis cystic fibrosis cystitis degeneration of macula and posterior pole dengue disease dengue hemorrhagic fever dental caries dentin caries dermatitis dermatomyositis dermatophytosis diabetes insipidus diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease by infectious agent disseminated intravascular coagulation distal myopathy eclampsia embryoma encephalomyelitis end stage renal disease endometrial cancer endometrial carcinoma endomyocardial fibrosis enterobiasis epilepsy esophagus squamous cell carcinoma essential hypertension facioscapulohumeral muscular dystrophy fetal erythroblastosis filariasis follicular lymphoma fungal infectious disease gallbladder disease gastroenteritis gastrointestinal tularemia gestational diabetes giardiasis gliosarcoma glomerulonephritis glucose intolerance goiter gonadal dysgenesis heart disease hemiplegia hemolytic-uremic syndrome hepatitis B hepatitis C hepatitis hepatocellular carcinoma hereditary angioedema herpes simplex high grade glioma histoplasmosis human immunodeficiency virus infectious disease hypereosinophilic syndrome hyperglycemia hyperhomocysteinemia hypersensitivity vasculitis hypertension hyperthyroidism hypertrophic cardiomyopathy hypothyroidism ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease immunoglobulin alpha deficiency inflammatory bowel disease 1 inflammatory bowel disease influenza intermediate coronary syndrome intestinal schistosomiasis intrinsic asthma invasive aspergillosis irritable bowel syndrome juvenile polyposis syndrome juvenile rheumatoid arthritis keratoconjunctivitis sicca kidney disease kidney failure large intestine cancer legionellosis leishmaniasis lepromatous leprosy leprosy leptospirosis leukemia leukopenia limb-girdle muscular dystrophy liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lupus erythematosus lupus nephritis lymphoblastic lymphoma lymphoma macrocytic anemia macular degeneration malaria membranous glomerulonephritis meningitis meningococcal meningitis miliary tuberculosis mixed glioma multiple myeloma multiple sclerosis muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myositis myxedema narcolepsy nephritis nephrosis nervous system disease neurocirculatory asthenia neurogenic arthropathy neurohypophyseal diabetes insipidus neuropathy neutropenia newborn respiratory distress syndrome non-suppurative otitis media nutmeg liver obesity 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 type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive lung disease oculopharyngeal muscular dystrophy oral candidiasis osteoporosis otitis media ovarian cancer pancreatitis panic disorder parapsoriasis patent ductus arteriosus pemphigus vulgaris pemphigus perinatal necrotizing enterocolitis periodontal disease periodontitis periodontosis peripheral nervous system disease peripheral vascular disease placental insufficiency pneumonia polymyalgia rheumatica pre-eclampsia prediabetes syndrome primary biliary cholangitis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary cutaneous T-cell non-Hodgkin lymphoma primary immunodeficiency disease primary open angle glaucoma prostate cancer prostate carcinoma protein C deficiency protein S deficiency psoriasis psoriatic arthritis pulmonary fibrosis pulmonary tuberculosis purpura fulminans pustulosis of palm and sole pyoureter renal osteodystrophy respiratory allergy respiratory failure rheumatic fever rheumatoid arthritis rhinitis rippling muscle disease 2 schistosomiasis selective IgA deficiency disease selective IgG deficiency disease sensorineural hearing loss severe acute respiratory syndrome severe congenital neutropenia sickle cell anemia silent myocardial infarction spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spondyloarthropathy spondylosis sporotrichosis stomach cancer stomach carcinoma sudden infant death syndrome superficial mycosis systemic lupus erythematosus systemic primary carnitine deficiency disease temporal arteritis thrombocytopenia thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyrotoxicosis tonsillitis tooth agenesis toxic shock syndrome trichinosis trigonitis trypanosomiasis tuberculosis tuberculous pneumothorax 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 ulcerative colitis uremia urinary schistosomiasis urinary tract obstruction uterine cancer uterine corpus cancer vaginitis vascular disease vasculitis vasomotor rhinitis viral infectious disease viral meningitis visceral leishmaniasis visual epilepsy vitiligo vulvitis vulvovaginal candidiasis vulvovaginitis white piedra yellow fever
5111	proliferating cell nuclear antigen	PCNA	Homo sapiens (human)	Lewy body dementia ataxia-telangiectasia-like disorder-2 brain ischemia hepatocellular carcinoma hypothyroidism invasive ductal carcinoma leiomyoma liver cancer mucositis nephroblastoma obstructive jaundice osteoporosis renal cell carcinoma sciatic neuropathy seminoma stomach cancer transient cerebral ischemia
276	amylase alpha 1A	AMY1A	Homo sapiens (human)	McCune Albright syndrome Sjogren's syndrome Zollinger-Ellison syndrome adenocarcinoma adenoma allergic rhinitis anorexia nervosa anxiety disorder autism spectrum disorder autistic disorder cancer cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma essential hypertension generalized anxiety disorder granular cell carcinoma hepatocellular carcinoma hyperinsulinism hypertension hypothalamic disease inflammatory bowel disease 1 inflammatory bowel disease intellectual disability keratoconjunctivitis sicca kwashiorkor learning disability liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder marasmus meconium aspiration syndrome melancholic depression multiple myeloma neurotic disorder nutrition disease obesity obsolete melancholia obstructive sleep apnea parathyroid gland disease periodontal disease phobic disorder post-traumatic stress disorder protein-energy malnutrition schizophrenia seasonal affective disorder substance abuse substance-related disorder tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis
51167	cytochrome b5 reductase 4	CYB5R4 Aliases: b5+b5R dJ676J13.1	Homo sapiens (human)	breast cancer diabetes mellitus diabetic ketoacidosis gestational diabetes glucose intolerance maturity-onset diabetes of the young prediabetes syndrome type 2 diabetes mellitus
1557	cytochrome P450 family 2 subfamily C member 19	CYP2C19 Aliases: CPCJ P450IIC19	Homo sapiens (human)	Behcet's disease Keshan disease Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Plasmodium falciparum malaria SADDAN Schwartz-Jampel syndrome 1 Stevens-Johnson syndrome Sveinsson chorioretinal atrophy Unverricht-Lundborg syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute chest syndrome acute kidney failure acute lymphoblastic leukemia acute monocytic leukemia acute myocardial infarction age related macular degeneration agranulocytosis alcoholic liver cirrhosis allergic asthma androgen insensitivity syndrome anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease aspergillosis asthma atherosclerosis atrial fibrillation atrophic gastritis autism spectrum disorder autistic disorder autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome biliary tract cancer black piedra bladder carcinoma blepharospasm brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cardiovascular system disease carotid artery thrombosis carotid stenosis cerebral artery occlusion cerebral infarction cerebrovascular disease cholestasis chronic kidney disease coccidioidomycosis colorectal cancer colorectal carcinoma common cold congenital adrenal hyperplasia congenital diaphragmatic hernia congenital intrinsic factor deficiency congestive heart failure coronary artery disease coronary thrombosis cystic fibrosis degeneration of macula and posterior pole depressive disorder developmental and epileptic encephalopathy 2 diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy disease of mental health disease of metabolism duodenal ulcer dysthymic disorder early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma endometriosis of uterus endometriosis endomyocardial fibrosis eosinophilic esophagitis epilepsy erythema multiforme esophageal cancer esophageal carcinoma esophagitis esophagus squamous cell carcinoma essential hypertension essential tremor eye disease familial hyperlipidemia familial nephrotic syndrome focal hand dystonia gallbladder disease gastric ulcer gastritis gastroesophageal reflux disease gastrointestinal system cancer generalized anxiety disorder glomerulonephritis head and neck cancer head and neck squamous cell carcinoma heart disease hematologic cancer hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma heroin dependence hiatus hernia histoplasmosis hypereosinophilic syndrome hypertension hypertrophic cardiomyopathy hypochondroplasia immune system disease inclusion body myositis inflammatory bowel disease 1 inflammatory bowel disease intermediate coronary syndrome intermittent claudication intracranial aneurysm intrinsic asthma invasive aspergillosis kidney disease kidney failure large intestine cancer laryngeal carcinoma larynx cancer leukopenia lipoid nephrosis liver cancer liver cirrhosis liver disease lobular neoplasia lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus nephritis macular degeneration major depressive disorder malaria melancholic depression multiple chemical sensitivity multiple epiphyseal dysplasia multiple myeloma multiple sclerosis myocardial infarction nephritis nephrosis nephrotic syndrome neurotic disorder neutropenia nutmeg liver obsessive-compulsive disorder obsolete dyspepsia obsolete infantile epileptic encephalopathy obsolete melancholia osteochondrodysplasia pancreatic cancer pancreatic carcinoma panic disorder parapsoriasis patent ductus arteriosus peptic esophagitis peptic ulcer disease peripheral vascular disease pharyngitis phobic disorder premature menopause primary open angle glaucoma primary ovarian insufficiency prostate cancer prostate carcinoma psoriasis psoriatic arthritis psychotic disorder pustulosis of palm and sole pyoureter retinal disease retinitis rheumatoid arthritis schizophrenia severe congenital neutropenia sickle cell anemia silent myocardial infarction sporotrichosis squamous cell carcinoma stomach cancer stomach carcinoma substance abuse substance-related disorder sudden infant death syndrome superficial mycosis systemic lupus erythematosus tongue squamous cell carcinoma transient cerebral ischemia tuberculosis type 2 diabetes mellitus ulcerative colitis urinary bladder cancer vasculitis vertebrobasilar insufficiency visual epilepsy white piedra
26280	interleukin 1 receptor accessory protein like 2	IL1RAPL2 Aliases: IL-1R9 IL1R9 IL1RAPL-2 TIGIRR-1	Homo sapiens (human)	autism spectrum disorder autistic disorder breast cancer childhood type dermatomyositis dermatomyositis hepatitis C myositis
8460	tyrosylprotein sulfotransferase 1	TPST1 Aliases: TANGO13A transport and golgi organization 13 homolog A (Drosophila)	Homo sapiens (human)	bronchus cancer bronchus carcinoma cancer colorectal adenocarcinoma colorectal cancer colorectal carcinoma gout large intestine cancer lung benign neoplasm lung cancer lung carcinoma
220	aldehyde dehydrogenase 1 family member A3	ALDH1A3 Aliases: RALDH3 retinaldehyde dehydrogenase 3	Homo sapiens (human)	Marfan syndrome Meckel syndrome 1 Meckel syndrome acoustic neuroma adenocarcinoma adenoma angiomatous meningioma autism spectrum disorder autistic disorder benign meningioma bilateral optic nerve hypoplasia bile duct adenocarcinoma bile duct carcinoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral convexity meningioma choanal atresia cholangiocarcinoma clear cell meningioma coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma distal arthrogryposis embryoma familial adenomatous polyposis 1 familial adenomatous polyposis fibrous meningioma gallbladder cancer gallbladder carcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma high grade glioma intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma islet cell tumor isolated microphthalmia 1 isolated microphthalmia 2 isolated microphthalmia 3 isolated microphthalmia 4 isolated microphthalmia 6 isolated microphthalmia 7 isolated microphthalmia 8 large intestine cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma malignant pleural mesothelioma melanoma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma neuroblastoma olfactory groove meningioma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma pituitary adenoma polycystic ovary syndrome prostate cancer prostate carcinoma psammomatous meningioma rheumatoid arthritis secretory meningioma seminoma situs inversus skin melanoma spinal meningioma steatotic liver disease stomach cancer stomach carcinoma testicular cancer testicular germ cell cancer thyroid gland papillary carcinoma transitional meningioma transthyretin amyloidosis tuberous sclerosis tubular adenocarcinoma
3820	killer cell lectin like receptor B1	KLRB1 Aliases: CD161 CLEC5B NKR-P1 NKR-P1A hNKR-P1A natural killer cell surface protein P1A	Homo sapiens (human)	Goodpasture syndrome Takayasu's arteritis acquired immunodeficiency syndrome acute promyelocytic leukemia aggressive NK-cell leukemia allergic asthma arthritis arthropathy asthma autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bone disease bronchus cancer bronchus carcinoma cancer cartilage disease cataract connective tissue disease eclampsia embryoma familial multiple nevi flammei granulomatosis with polyangiitis hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hidradenitis suppurativa hidradenitis human immunodeficiency virus infectious disease immune system disease influenza intermittent claudication intrinsic asthma liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 melanoma mitral valve stenosis multiple myeloma multiple sclerosis myocarditis osteoarthritis peeling skin syndrome periodontitis placental insufficiency pneumonia polyarteritis nodosa pompholyx prostate cancer prostate carcinoma psoriatic arthritis rheumatoid arthritis scleroderma skin melanoma spondyloarthropathy spondylosis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma tuberculosis urinary bladder cancer viral infectious disease
79411	galactosidase beta 1 like	GLB1L Aliases: MGC10771	Homo sapiens (human)
27293	sphingomyelin phosphodiesterase acid like 3B	SMPDL3B Aliases: ASML3B	Homo sapiens (human)	Moyamoya disease focal segmental glomerulosclerosis glomerulonephritis kidney disease nephritis nephrosis pyoureter
3251	hypoxanthine phosphoribosyltransferase 1	HPRT1 Aliases: HGPRT Lesch-Nyhan syndrome hypoxanthine guanine phosphoribosyl transferase	Homo sapiens (human)	Alzheimer's disease Borjeson-Forssman-Lehmann syndrome CD40 ligand deficiency Creutzfeldt-Jakob disease Duchenne muscular dystrophy Ewing sarcoma Fanconi anemia complementation group A Fanconi anemia Guillain-Barre syndrome HRPT-related hyperuricemia Laron syndrome Lesch-Nyhan syndrome Marfan syndrome Miller Fisher syndrome Rett syndrome Simpson-Golabi-Behmel syndrome type 1 T-cell acute lymphoblastic leukemia X-linked dilated cardiomyopathy X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 achondroplasia acoustic neuroma acquired polycythemia acute biphenotypic leukemia acute kidney failure acute leukemia acute lymphoblastic leukemia acute myeloid leukemia acute promyelocytic leukemia adult acute lymphocytic leukemia adult fibrosarcoma agnosia alternating hemiplegia of childhood anemia angiomatous meningioma arthritis arthropathy aspartylglucosaminuria ataxia telangiectasia atrophy of testis attention deficit hyperactivity disorder autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy bacterial sepsis basal ganglia disease benign meningioma blepharospasm bone disease bone marrow cancer bone marrow disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence cartilage disease central nervous system disease central nervous system lymphoma cerebral convexity meningioma cerebral palsy childhood acute lymphocytic leukemia childhood leukemia childhood type dermatomyositis choriocarcinoma chronic fatigue syndrome chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy chronic myeloid leukemia clear cell meningioma colitis collagen disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer connective tissue disease demyelinating disease dermatomyositis developmental coordination disorder diabetic ketoacidosis dilated cardiomyopathy 1A 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 dysplastic nevus syndrome dystonia embryoma encephalitis encephalomyelitis endometrial stromal sarcoma endometriosis of uterus endometriosis epilepsy epithelioid sarcoma erythropoietin polycythemia esophageal cancer esophageal carcinoma familial erythrocytosis 2 fibrosarcoma fibrous meningioma focal hand dystonia frozen shoulder fucosidosis galactosialidosis gastroenteritis giardiasis glomerulonephritis glycoproteinosis gout hematopoietic system disease hemiplegia hepatoblastoma hepatocellular carcinoma herpes simplex histiocytosis hyperglycemia hyperuricemia ileitis ileocolitis immune system disease inflammatory bowel disease inherited metabolic disorder intellectual disability intrahepatic cholestasis of pregnancy intraorbital meningioma intraventricular meningioma kidney disease kidney failure large intestine cancer learning disability leukemia leukopenia lingual-facial-buccal dyskinesia liver cancer lobular neoplasia lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoblastic lymphoma lymphoma lymphoplasmacyte-rich meningioma macrocytic anemia malaria measles megaloblastic anemia melanoma meningioma meningothelial meningioma microcystic meningioma middle cerebral artery infarction movement disease multiple sclerosis muscular dystrophy myelitis myeloproliferative neoplasm myositis neovascular inflammatory vitreoretinopathy nephritis nephrolithiasis nephrosis nervous system disease neuroblastoma non-syndromic X-linked intellectual disability obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculocerebrorenal syndrome olfactory groove meningioma osteoarthritis osteoporosis ovarian cancer papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma paroxysmal nocturnal hemoglobinuria pituitary adenoma placenta cancer pleomorphic adenoma polycythemia prostate cancer prostate carcinoma psammomatous meningioma purine-pyrimidine metabolic disorder pyoureter relapsing-remitting multiple sclerosis rheumatoid arthritis sarcoma scleroderma secretory meningioma situs inversus skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal cord disease spinal meningioma spindle cell sarcoma stress polycythemia syringomyelia systemic lupus erythematosus systemic scleroderma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma transitional meningioma tropical spastic paraparesis tuberculosis tuberous sclerosis 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 uric acid nephrolithiasis uterine corpus sarcoma visual epilepsy xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
1558	cytochrome P450 family 2 subfamily C member 8	CYP2C8 Aliases: CPC8	Homo sapiens (human)	Ewing sarcoma Plasmodium falciparum malaria acute lymphoblastic leukemia acute myocardial infarction agranulocytosis allergic asthma alternating hemiplegia of childhood anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis autonomic neuropathy bacterial sepsis breast cancer breast carcinoma cancer central nervous system disease cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia chronic kidney disease chronic myeloid leukemia coronary artery disease coronary thrombosis diabetes mellitus embryoma end stage renal disease essential hypertension essential tremor gastrointestinal stromal tumor glomerulonephritis gout hepatocellular carcinoma hypertension hypoglycemia intrinsic asthma kidney disease leukopenia liver cancer lung cancer lung non-small cell carcinoma lymphoblastic lymphoma macrocytic anemia malaria middle cerebral artery infarction multiple myeloma myocardial infarction nephritis nephrosis nervous system disease neuropathy neutropenia nutmeg liver osteonecrosis ovarian cancer ovarian carcinoma peptic ulcer disease peripheral nervous system disease polyneuropathy prostate cancer prostate carcinoma pseudosarcomatous fibromatosis pyoureter renal hypertension severe congenital neutropenia silent myocardial infarction squamous cell carcinoma sudden infant death syndrome thrombocytopenia tongue squamous cell carcinoma type 2 diabetes mellitus
1178	Charcot-Leyden crystal galectin	CLC Aliases: Gal-10 LGALS10 MGC149659 eosinophil lysophospholipase galectin 10 lectin, galactoside-binding, soluble, 10 lysolecithin acylhydrolase	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 Dent disease Pick's disease Reye syndrome acute myeloid leukemia allergic asthma allergic rhinitis arthritis arthropathy asthma autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 blindness cancer celiac disease central nervous system cancer cerebral degeneration chronic ethmoiditis chronic sphenoidal sinusitis colorectal cancer colorectal carcinoma corneal disease craniosynostosis embryoma eosinophilic esophagitis epilepsy essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis gliosarcoma glomerulonephritis high grade glioma hypertension immune system disease intrinsic asthma islet cell tumor keratoconus kidney disease large intestine cancer male infertility mixed glioma myasthenia gravis myotonia congenita nasopharynx carcinoma nephritis nephrolithiasis nephrosis osteoarthritis osteopetrosis osteoporosis osteosclerosis parapsoriasis psoriasis pustulosis of palm and sole pyoureter thyroid gland anaplastic carcinoma uric acid nephrolithiasis vasomotor rhinitis
683	bone marrow stromal cell antigen 1	BST1 Aliases: ADP-ribosyl cyclase 2 BST-1 CD157 NAD(+) nucleosidase cADPR2 cyclic ADP-ribose hydrolase	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 Burkitt lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome acute monocytic leukemia acute myeloid leukemia allergic asthma asthma autism spectrum disorder autistic disorder benign mesothelioma benign pleural mesothelioma bronchus cancer bronchus carcinoma cancer cerebral degeneration chronic lymphocytic leukemia depressive disorder dysthymic disorder embryoma essential hypertension hypertension inflammatory and toxic neuropathy intrinsic asthma lung benign neoplasm lung cancer lung carcinoma lung disease major depressive disorder malignant mesothelioma malignant pleural mesothelioma melancholic depression neurotic disorder obsolete melancholia ovarian cancer ovarian carcinoma paroxysmal nocturnal hemoglobinuria pleural tuberculosis pneumonia prion disease prostate cancer prostate carcinoma tuberculosis
280	amylase alpha 2B	AMY2B	Homo sapiens (human)	autosomal recessive congenital ichthyosis 1 ichthyosis keratosis follicularis lung benign neoplasm lung carcinoma mongolian spot obsolete congenital ichthyosiform erythroderma pseudoxanthoma elasticum
109703458	hydroxyacyl-thioester dehydratase type 2	HTD2	Homo sapiens (human)	rheumatoid arthritis
414328	IDNK gluconokinase	IDNK Aliases: bA522I20.2 hGntK	Homo sapiens (human)
5161	pyruvate dehydrogenase E1 subunit alpha 2	PDHA2	Homo sapiens (human)	Marfan syndrome azoospermia disease of metabolism male infertility pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency retinal degeneration situs inversus spermatogenic failure 1 spermatogenic failure tuberous sclerosis
64834	ELOVL fatty acid elongase 1	ELOVL1 Aliases: Ssc1	Homo sapiens (human)	Cauda equina syndrome acanthosis nigricans acrodermatitis adrenoleukodystrophy cancer dermatitis dry eye syndrome hyperglycemia neurogenic bladder obsolete asthenopia xerophthalmia
2641	glucagon	GCG	Homo sapiens (human)	Alzheimer's disease prediabetes syndrome
226	aldolase, fructose-bisphosphate A	ALDOA	Homo sapiens (human)	Laron syndrome abdominal obesity-metabolic syndrome 1 achondroplasia arthritis arthropathy bile duct adenocarcinoma bile duct cancer bile duct carcinoma bone osteosarcoma breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma childhood osteosarcoma cholangiocarcinoma cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital hemolytic anemia congenital ptosis coronary artery disease cystinuria embryoma favism 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 hemoglobinopathy hemolytic anemia hepatocellular carcinoma hereditary elliptocytosis intrahepatic cholangiocarcinoma invasive ductal carcinoma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma nonpapillary renal cell carcinoma normocytic anemia obstructive sleep apnea osteoarthritis osteosarcoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma ptosis renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma spondyloarthropathy spondylosis

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