congenital ichthyosiform erythroderma Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_1699)
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Genes

6 genes involed in the disease congenital ichthyosiform erythroderma from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
ALOX12B arachidonate 12-lipoxygenase, 12R type
ALOXE3 arachidonate lipoxygenase 3
CYP4F22 cytochrome P450, family 4, subfamily F, polypeptide 22
NIPAL4 NIPA-like domain containing 4
TGM1 transglutaminase 1