aplasia/hypoplasia involving the sinuses Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of a cranial sinus or sinuses. (Human Phenotype Ontology, HP_0009120)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009120
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Genes

12 genes associated with the aplasia/hypoplasia involving the sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGA aspartylglucosaminidase
ALX3 ALX homeobox 3
AMER1 APC membrane recruitment protein 1
ATRX alpha thalassemia/mental retardation syndrome X-linked
COL11A1 collagen, type XI, alpha 1
CTSK cathepsin K
DNAI1 dynein, axonemal, intermediate chain 1
FLNA filamin A, alpha
FUCA1 fucosidase, alpha-L- 1, tissue
NOTCH2 notch 2
RUNX2 runt-related transcription factor 2
TRIM37 tripartite motif containing 37