Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Methionine Adenosyltransferase Deficiency MAT1A disease C0268621 GeneticVariation 0.78 orphanet , disgenet
Methionine Adenosyltransferase Deficiency MAT1A disease C0268621 AlteredExpression 0.78 orphanet , disgenet
Methionine Adenosyltransferase Deficiency MAT1A disease C0268621 CausalMutation 0.78 orphanet , disgenet
Methionine Adenosyltransferase Deficiency MAT1A disease C0268621 Biomarker 0.78 orphanet , disgenet
Methionine Adenosyltransferase Deficiency MAT1A disease C0268621 GermlineCausalMutation 0.78 orphanet , disgenet
Methionine Adenosyltransferase Deficiency AHCY disease C0268621 Biomarker 0.3 disgenet
Methionine Adenosyltransferase Deficiency GNMT disease C0268621 Biomarker 0.3 disgenet
Methionine Adenosyltransferase Deficiency ACAT1 disease C0268621 Biomarker 0.02 disgenet
Methionine Adenosyltransferase Deficiency ACAT1 disease C0268621 GeneticVariation 0.02 disgenet
Methionine Adenosyltransferase Deficiency CBS disease C0268621 AlteredExpression 0.02 disgenet
Methionine Adenosyltransferase Deficiency ADK disease C0268621 Biomarker 0.02 disgenet
Methionine Adenosyltransferase Deficiency CBS disease C0268621 Biomarker 0.02 disgenet
Methionine Adenosyltransferase Deficiency ADK disease C0268621 GeneticVariation 0.02 disgenet
Methionine Adenosyltransferase Deficiency MAT2A disease C0268621 GeneticVariation 0.01 disgenet
Methionine Adenosyltransferase Deficiency MCCD1 disease C0268621 GeneticVariation 0.01 disgenet
Methionine Adenosyltransferase Deficiency MMP2 disease C0268621 AlteredExpression 0.01 disgenet
Methionine Adenosyltransferase Deficiency MNAT1 disease C0268621 GeneticVariation 0.01 disgenet
Methionine Adenosyltransferase Deficiency SPP1 disease C0268621 AlteredExpression 0.01 disgenet
Methionine Adenosyltransferase Deficiency PEA15 disease C0268621 GeneticVariation 0.01 disgenet
Methionine Adenosyltransferase Deficiency FAH disease C0268621 Biomarker 0.01 disgenet
Methionine Adenosyltransferase Deficiency ALG1 disease C0268621 GeneticVariation 0.01 disgenet
Methionine Adenosyltransferase Deficiency CBSL disease C0268621 AlteredExpression 0.01 disgenet
Methionine Adenosyltransferase Deficiency IL6 disease C0268621 AlteredExpression 0.01 disgenet
Methionine Adenosyltransferase Deficiency MET NA C0268621 NA NA orphanet
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