Zlotogora-Ogur Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Zlotogora-Ogur syndrome is an ectodermal dysplasia syndrome characterized by hair, skin and teeth anomalies, facial dysmophism with cleft lip and palate, cutaneous syndactyly and, in some cases, intellectual disability. (Orphanet Rare Disease Ontology, Orphanet_3253)
External Link https://www.disgenet.org/browser/0/1/0/C2931488
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Genes

5 genes associated with the disease Zlotogora-Ogur Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
GRHL2 grainyhead-like 2 (Drosophila)
IRF6 interferon regulatory factor 6
NECTIN1 nectin cell adhesion molecule 1
PVR poliovirus receptor
WNT10A wingless-type MMTV integration site family, member 10A