Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "A"

111 to 120 of 1170 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
111	34	ACADM	Acyl-CoA dehydrogenase medium chain	ACAD1, MCAD, MCADH	Enterocolitis, Congenital hydrocephalus, Liver failure, Obesity, Infantile spasms
112	35	ACADS	Acyl-CoA dehydrogenase short chain	ACAD3, SCAD	Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cannabis abuse, Congestive heart failure, Butyryl-coa dehydrogenase deficiency, Heart failure, Major depressive disorder, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome, Diabetes mellitus type 2
113	36	ACADSB	Acyl-CoA dehydrogenase short/branched chain	2-MEBCAD, ACAD7, SBCAD	2-methylbutyryl-coa dehydrogenase deficiency, Autism, Lewy body disease, Periodontitis, Rheumatic disease
114	37	ACADVL	Acyl-CoA dehydrogenase very long chain	ACAD6, LCACD, VLCAD	Autism, Cardiac arrhythmia, Dilated cardiomyopathy, Cardiomyopathy, Hearing loss, Hypoxia, Intellectual developmental disorder, Myopathy, Very long chain acyl-coa dehydrogenase deficiency, Very long-chain acyl-coa dehydrogenase deficiency, Yorifuji okuno syndrome
115	176	ACAN	Aggrecan	AGC1, AGCAN, CSPG1, CSPGCP, MSK16, SEDK, SSOAOD	Short stature spectrum, Aortic stenosis, Aortic valve disease, Rheumatoid arthritis, Color vision deficiency, Desbuquois syndrome, Dupuytren contracture, Hearing loss, Meniere disease, Obesity, Osteoarthritis, Spondyloepimetaphyseal dysplasia, Spondyloepiphyseal dysplasia
116	9744	ACAP1	ArfGAP with coiled-coil, ankyrin repeat and PH domains 1	CENTB1	Autoimmune thyroid disease, Hypothyroidism, Systemic lupus erythematosus, Thyroid disease, Diabetes mellitus type 1, Diabetes mellitus type 2
117	23527	ACAP2	ArfGAP with coiled-coil, ankyrin repeat and PH domains 2	CENTB2, CNT-B2	Bone fracture, Glomerulonephritis, Kidney disease, Metabolic syndrome, Prostate cancer, Diabetes mellitus type 2
118	38	ACAT1	Acetyl-CoA acetyltransferase 1	ACAT, MAT, T2, THIL	Beta-ketothiolase deficiency, Carbohydrate metabolism disease, Acetyl-coa acetyltransferase deficiency, Disorder of carbohydrate metabolism, Kidney failure, Liver cirrhosis, Seizures
119	39	ACAT2	Acetyl-CoA acetyltransferase 2	-	Acetyl-coa acetyltransferase deficiency, Ischemic heart disease, Coronary artery disease, Cytosolic acetoacetyl-coa thiolase deficiency, Myocardial ischemia
120	64746	ACBD3	Acyl-CoA binding domain containing 3	GCP60, GOCAP1, GOLPH1, PAP7	Astrocytoma, Glioma

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