Associated diseases for pathway:

Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5)

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disease(s) associated

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Related Pathways Pathways (KEGG or Reactome) that share the most genes with Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5).
4
Miscellaneous substrates 1 shared geneCYP4F22 Related via 1 shared gene including CYP4F22. Eicosanoids 1 shared geneCYP4F22 Related via 1 shared gene including CYP4F22. Fatty acids 1 shared geneCYP4F22 Related via 1 shared gene including CYP4F22. Synthesis of Leukotrienes (LT) and Eoxins (EX) 1 shared geneCYP4F22 Related via 1 shared gene including CYP4F22.
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