Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "A"

561 to 570 of 1170 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
561	9949	AMMECR1	AMMECR nuclear protein 1	AMMERC1, MFHIEN	Alport syndrome, Desbuquois syndrome, Midface hypoplasia-hearing impairment-elliptocytosis-nephrocalcinosis syndrome
562	83607	AMMECR1L	AMMECR1 like	-	Alzheimer disease
563	81693	AMN	Amnion associated transmembrane protein	IGS2, PRO1028, amnionless	Megaloblastic anemia, Anxiety disorder, Edema, Extravasation of diagnostic and therapeutic materials, Imerslund-grasbeck syndrome, Kidney failure, Post-traumatic stress disorder, Diabetes mellitus type 2, Vitamin b deficiency
564	154796	AMOT	Angiomotin	-	Brain neoplasms
565	154810	AMOTL1	Angiomotin like 1	CFCHS, JEAP	Basal cell carcinoma, Cleft lip and palate, Craniofaciocardiohepatic syndrome, Glioma, Auricle malformation, Non-melanoma skin carcinoma, Orofacial cleft, Tethered cord syndrome
566	270	AMPD1	Adenosine monophosphate deaminase 1	MAD, MADA, MMDD	Myoadenylate deaminase deficiency, Autism, Ischemic heart disease, Congestive heart failure, Coronary artery disease, Heart failure, Hyperlipoproteinemia, Ovarian epithelial cancer, Myocardial ischemia, Myopathy, Ovarian cancer
567	271	AMPD2	Adenosine monophosphate deaminase 2	AMPD, PCH9, SPG63	Autoimmune thrombocytopenic purpura, Spastic paraplegia, Breast cancer, Congenital brain malformation, Congenital hypoplasia of part of brain, Congenital neurologic anomalies, Estrogen-receptor negative breast cancer, Global developmental delay, Hydranencephaly, Intellectual developmental disorder, Lissencephaly, Macrogyria, Microgyria, Pontocerebellar hypoplasia, Spastic ataxia, Hereditary spastic paraplegia View all (1 more)
568	272	AMPD3	Adenosine monophosphate deaminase 3	-	Myoadenylate deaminase deficiency, Atrial fibrillation, Bipolar disorder, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Melanoma, Erythrocyte amp deaminase deficiency, Hemorrhoid, Hypertension, Major depressive disorder, Nephrolithiasis, Osteoarthritis, Scoliosis
569	273	AMPH	Amphiphysin	AMPH1	Scoliosis, Small vessel stroke
570	275	AMT	Aminomethyltransferase	GCE, GCE2, GCST, GCVT, NKH	Glycine encephalopathy, Hyperglycemia

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