Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Benign Fibrous Histiocytoma AKT1 disease C0206644 CausalMutation 0.3 disgenet
Benign Fibrous Histiocytoma MMP21 disease C0206644 Biomarker 0.3 disgenet
Benign Fibrous Histiocytoma ALK disease C0206644 GeneticVariation 0.05 disgenet
Benign Fibrous Histiocytoma ALK disease C0206644 AlteredExpression 0.05 disgenet
Benign Fibrous Histiocytoma ALK disease C0206644 Biomarker 0.05 disgenet
Benign Fibrous Histiocytoma PRKCD disease C0206644 GeneticVariation 0.02 disgenet
Benign Fibrous Histiocytoma PRKCD disease C0206644 Biomarker 0.02 disgenet
Benign Fibrous Histiocytoma MCM2 disease C0206644 AlteredExpression 0.01 disgenet
Benign Fibrous Histiocytoma FGFR2 disease C0206644 AlteredExpression 0.01 disgenet
Benign Fibrous Histiocytoma MKI67 disease C0206644 Biomarker 0.01 disgenet
Benign Fibrous Histiocytoma CD34 disease C0206644 Biomarker 0.01 disgenet
Benign Fibrous Histiocytoma LAMTOR1 disease C0206644 Biomarker 0.01 disgenet
Benign Fibrous Histiocytoma MOV10L1 disease C0206644 GeneticVariation 0.01 disgenet
Benign Fibrous Histiocytoma TP53 disease C0206644 Biomarker 0.01 disgenet
Benign Fibrous Histiocytoma EWSR1 disease C0206644 AlteredExpression 0.01 disgenet
Benign Fibrous Histiocytoma NUMA1 disease C0206644 Biomarker 0.01 disgenet
Benign Fibrous Histiocytoma ACVRL1 disease C0206644 AlteredExpression 0.01 disgenet
Benign Fibrous Histiocytoma MIB1 disease C0206644 Biomarker 0.01 disgenet
Benign Fibrous Histiocytoma SMUG1 disease C0206644 Biomarker 0.01 disgenet
Benign Fibrous Histiocytoma KIRREL1 disease C0206644 GeneticVariation 0.01 disgenet
Benign Fibrous Histiocytoma CREB1 disease C0206644 AlteredExpression 0.01 disgenet
Benign Fibrous Histiocytoma CHAMP1 disease C0206644 GeneticVariation 0.01 disgenet
Benign Fibrous Histiocytoma SFMBT1 disease C0206644 Biomarker 0.01 disgenet
Benign Fibrous Histiocytoma PRKCA disease C0206644 GeneticVariation 0.01 disgenet
Benign Fibrous Histiocytoma SLPI disease C0206644 AlteredExpression 0.01 disgenet
Benign Fibrous Histiocytoma PRKCB disease C0206644 GeneticVariation 0.01 disgenet
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