Rapp-Hodgkin Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal dominant disease characterized by abnormal development of ectodermal tissues including the skin, hair, nails, teeth and sweat glands and anhidrotic ectodermal dysplasia with cleft lip/palate. (Human Disease Ontology, DOID_0060330)
External Link https://www.disgenet.org/browser/0/1/0/C1785148
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Genes

9 genes associated with the disease Rapp-Hodgkin Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CKAP4 cytoskeleton-associated protein 4
COX8A cytochrome c oxidase subunit VIIIA (ubiquitous)
DHCR7 7-dehydrocholesterol reductase
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
RPE65 retinal pigment epithelium-specific protein 65kDa
TAT tyrosine aminotransferase
TP63 tumor protein p63
UVRAG UV radiation resistance associated