Mesoaxial Polydactyly Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The presence of a supernumerary finger or toe (not a thumb or hallux) involving the third or fourth metacarpal/tarsal with associated osseous syndactyly. (Human Phenotype Ontology, HP_0100260)
External Link https://www.disgenet.org/browser/0/1/0/C1848595
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Genes

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

Symbol Name
C5ORF42 chromosome 5 open reading frame 42
FAM149B1 family with sequence similarity 149, member B1
KIAA0753 KIAA0753
KIF7 kinesin family member 7
LZTFL1 leucine zipper transcription factor-like 1
OFD1 oral-facial-digital syndrome 1
PDE6D phosphodiesterase 6D, cGMP-specific, rod, delta
TCTN3 tectonic family member 3
TMEM216 transmembrane protein 216