abnormality of the premaxilla Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the premaxilla. (Human Phenotype Ontology, HP_0010758)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010758
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6 genes associated with the abnormality of the premaxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COLEC11 collectin sub-family member 11
EFEMP2 EGF containing fibulin-like extracellular matrix protein 2
GLI2 GLI family zinc finger 2
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
PTCH1 patched 1