Pathways Knowlegdes
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| Pathway | DOIs | Note |
|---|---|---|
| Cholesterol biosynthesis with skeletal dysplasias Accession ID: WikiPathways:WP4804 |
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Rossi M, Hall CM, Bouvier R, Collardeau-Frachon S, Le Breton F, Bucourt M, Cordier MP, Vianey-Saban C, Parenti G, Andria G, Le Merrer M, Edery P, Offiah AC. Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesis. Pediatr Radiol. 2015 Jul;45(7):965–76. doi: 10.1007/s00247-014-3257-9. PMID: 25646736. |
| Mevalonic Aciduria Accession ID: PathBank:SMP0120794 |
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| CHILD Syndrome Accession ID: PathBank:SMP0120464 |
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| Desmosterolosis Accession ID: PathBank:SMP0120472 |
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| Lysosomal Acid Lipase Deficiency (Wolman Disease) Accession ID: PathBank:SMP0120512 |
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| Cholesteryl Ester Storage Disease Accession ID: PathBank:SMP0120573 |
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| Steroid Biosynthesis Accession ID: PathBank:SMP0000023 |
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| CHILD Syndrome Accession ID: PathBank:SMP0000387 |
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| Risedronate Action Pathway Accession ID: PathBank:SMP0000112 |
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| Cholesteryl Ester Storage Disease Accession ID: PathBank:SMP0000508 |
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| Steroid Biosynthesis Accession ID: PathBank:SMP0087326 |
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| Chondrodysplasia Punctata II, X-Linked Dominant (CDPX2) Accession ID: PathBank:SMP0120685 |
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| Hypercholesterolemia Accession ID: PathBank:SMP0120769 |
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| Hyper-IgD Syndrome Accession ID: PathBank:SMP0120793 |
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| Smith-Lemli-Opitz Syndrome (SLOS) Accession ID: PathBank:SMP0120515 |
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| Wolman Disease Accession ID: PathBank:SMP0120576 |
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| Smith-Lemli-Opitz Syndrome (SLOS) Accession ID: PathBank:SMP0000389 |
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| Lysosomal Acid Lipase Deficiency (Wolman Disease) Accession ID: PathBank:SMP0000319 |
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| Simvastatin Action Pathway Accession ID: PathBank:SMP0000082 |
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| Cerivastatin Action Pathway Accession ID: PathBank:SMP0000111 |
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