abnormal shape of the palpebral fissure Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of an abnormal shape of the palpebral fissure. (Human Phenotype Ontology, HP_0200005)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0200005
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Genes

4 genes associated with the abnormal shape of the palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NDN necdin, melanoma antigen (MAGE) family member
NSDHL NAD(P) dependent steroid dehydrogenase-like
SNRPN small nuclear ribonucleoprotein polypeptide N
UBE2A ubiquitin-conjugating enzyme E2A