Target Gene/Pathway Pathway / Gene

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KEGG PATHWAY
On map, Yellow: Drug target, Red: All disease-related

1

AMPK signaling pathway 💬

[1] HMGCR 💬

Lovastatin 💬

[11] 6 , 34, 46, 79, 156, 160, 195, 206, 263, 280, 310 💬

Disease ID	Name
6	Parkinson disease;Disease Parkinson's;
34	Neurofibromatosis;
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;
79	Homozygous familial hypercholesterolemia;
156	Rett syndrome;
160	Congenital ichthyosis;
195	Noonan syndrome;
206	Fragile X syndrome;
263	Cerebrotendinous xanthomatosis;27-hydroxylase deficiency;CYP27 deficiency;
280	Huge arteriovenous malformation with cervicofacial or limb lesion;Huge arteriovenous malformation;Arteriovenous malformation;
310	Congenital anomalies syndrome;

2

Bile secretion 💬

[1] HMGCR 💬

Lovastatin 💬

[11] 6 , 34, 46, 79, 156, 160, 195, 206, 263, 280, 310 💬

Disease ID	Name
6	Parkinson disease;Disease Parkinson's;
34	Neurofibromatosis;
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;
79	Homozygous familial hypercholesterolemia;
156	Rett syndrome;
160	Congenital ichthyosis;
195	Noonan syndrome;
206	Fragile X syndrome;
263	Cerebrotendinous xanthomatosis;27-hydroxylase deficiency;CYP27 deficiency;
280	Huge arteriovenous malformation with cervicofacial or limb lesion;Huge arteriovenous malformation;Arteriovenous malformation;
310	Congenital anomalies syndrome;

3

Bile secretion 💬

[1] NR1H4 💬

Chenodeoxycholic acid

[4] 20, 96, 234, 263 💬

Disease ID	Name
20	Adrenoleukodystrophy;ALD;
96	Crohn disease;Terminal ileitis;
234	Peroxisomal disease (except Adrenoleukodystrophy);Peroxisomal disease;Peroxisomal disorder;Peroxisome biogenesis disorder;
263	Cerebrotendinous xanthomatosis;27-hydroxylase deficiency;CYP27 deficiency;

4

Metabolic pathways 💬

[1] HMGCR 💬

Lovastatin 💬

[11] 6 , 34, 46, 79, 156, 160, 195, 206, 263, 280, 310 💬

Disease ID	Name
6	Parkinson disease;Disease Parkinson's;
34	Neurofibromatosis;
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;
79	Homozygous familial hypercholesterolemia;
156	Rett syndrome;
160	Congenital ichthyosis;
195	Noonan syndrome;
206	Fragile X syndrome;
263	Cerebrotendinous xanthomatosis;27-hydroxylase deficiency;CYP27 deficiency;
280	Huge arteriovenous malformation with cervicofacial or limb lesion;Huge arteriovenous malformation;Arteriovenous malformation;
310	Congenital anomalies syndrome;

5

Terpenoid backbone biosynthesis 💬

[1] HMGCR 💬

Lovastatin 💬

[11] 6 , 34, 46, 79, 156, 160, 195, 206, 263, 280, 310 💬

Disease ID	Name
6	Parkinson disease;Disease Parkinson's;
34	Neurofibromatosis;
46	Malignant rheumatoid arthritis;MRA;Rheumatoid vasculitis;RV;Rheumatoid arthritis;RA;
79	Homozygous familial hypercholesterolemia;
156	Rett syndrome;
160	Congenital ichthyosis;
195	Noonan syndrome;
206	Fragile X syndrome;
263	Cerebrotendinous xanthomatosis;27-hydroxylase deficiency;CYP27 deficiency;
280	Huge arteriovenous malformation with cervicofacial or limb lesion;Huge arteriovenous malformation;Arteriovenous malformation;
310	Congenital anomalies syndrome;

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