Pathways Knowlegdes
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| Pathway | DOIs | Note |
|---|---|---|
| Inner Membrane Transport Accession ID: PathBank:SMP0000808 |
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| Drug induction of bile acid pathway Accession ID: WikiPathways:WP2289 |
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| Drug induction of bile acid pathway Accession ID: WikiPathways:WP3253 |
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| Congenital Bile Acid Synthesis Defect Type III Accession ID: PathBank:SMP0120468 |
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| Congenital Bile Acid Synthesis Defect Type III Accession ID: PathBank:SMP0000318 |
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| Familial Hypercholanemia (FHCA) Accession ID: PathBank:SMP0120697 |
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| Cerebrotendinous Xanthomatosis (CTX) Accession ID: PathBank:SMP0120463 |
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| Congenital Bile Acid Synthesis Defect Type II Accession ID: PathBank:SMP0120467 |
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| Zellweger Syndrome Accession ID: PathBank:SMP0120495 |
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| Bile Acid Biosynthesis Accession ID: PathBank:SMP0000035 |
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| Congenital Bile Acid Synthesis Defect Type II Accession ID: PathBank:SMP0000314 |
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| Cerebrotendinous Xanthomatosis (CTX) Accession ID: PathBank:SMP0000315 |
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| Bile Acid Biosynthesis Accession ID: PathBank:SMP0087329 |
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| 27-Hydroxylase Deficiency Accession ID: PathBank:SMP0120652 |
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| Congenital Bile Acid Synthesis Defect Type III Accession ID: PathBank:SMP0120688 |
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| Familial Hypercholanemia (FHCA) Accession ID: PathBank:SMP0120477 |
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| Familial Hypercholanemia (FHCA) Accession ID: PathBank:SMP0000317 |
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| Bile Acid Biosynthesis Accession ID: PathBank:SMP0087236 |
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| Cerebrotendinous Xanthomatosis (CTX) Accession ID: PathBank:SMP0120683 |
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| Congenital Bile Acid Synthesis Defect Type II Accession ID: PathBank:SMP0120687 |
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