Abnormal Palmar Dermatoglyphics Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the dermatoglyphs, i.e., an abnormality of the patterns of ridges of the skin of palm of hand. (Human Phenotype Ontology, HP_0001018)
External Link https://www.disgenet.org/browser/0/1/0/C4025810
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Genes

5 genes associated with the disease Abnormal Palmar Dermatoglyphics in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BCOR BCL6 corepressor
CHD7 chromodomain helicase DNA binding protein 7
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
PORCN porcupine homolog (Drosophila)
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E