Pathways Knowlegdes

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Pathway DOIs Note
Biochemical pathways: part I

Accession ID: WikiPathways:WP3604
  • 10.1016/s0303-2647(98)00019-7
 Michal G. On representation of metabolic pathways. Biosystems. 1998 Jun;47(1-2):1–7. doi: 10.1016/s0303-2647(98)00019-7. PMID: 9715748.
Congenital Bile Acid Synthesis Defect Type III

Accession ID: PathBank:SMP0120468		 -
Congenital Bile Acid Synthesis Defect Type III

Accession ID: PathBank:SMP0000318		 -
Familial Hypercholanemia (FHCA)

Accession ID: PathBank:SMP0120697		 -
Cerebrotendinous Xanthomatosis (CTX)

Accession ID: PathBank:SMP0120463		 -
Congenital Bile Acid Synthesis Defect Type II

Accession ID: PathBank:SMP0120467		 -
Zellweger Syndrome

Accession ID: PathBank:SMP0120495		 -
Bile Acid Biosynthesis

Accession ID: PathBank:SMP0000035		 -
Congenital Bile Acid Synthesis Defect Type II

Accession ID: PathBank:SMP0000314		 -
Cerebrotendinous Xanthomatosis (CTX)

Accession ID: PathBank:SMP0000315		 -
Bile Acid Biosynthesis

Accession ID: PathBank:SMP0087329		 -
27-Hydroxylase Deficiency

Accession ID: PathBank:SMP0120652		 -
Congenital Bile Acid Synthesis Defect Type III

Accession ID: PathBank:SMP0120688		 -
Familial Hypercholanemia (FHCA)

Accession ID: PathBank:SMP0120477		 -
Familial Hypercholanemia (FHCA)

Accession ID: PathBank:SMP0000317		 -
Bile Acid Biosynthesis

Accession ID: PathBank:SMP0087236		 -
Cerebrotendinous Xanthomatosis (CTX)

Accession ID: PathBank:SMP0120683		 -
Congenital Bile Acid Synthesis Defect Type II

Accession ID: PathBank:SMP0120687		 -
Zellweger Syndrome

Accession ID: PathBank:SMP0120715		 -
27-Hydroxylase Deficiency

Accession ID: PathBank:SMP0120871		 -