abnormality of the parathyroid morphology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A structural abnormality of the parathyroid gland. (Human Phenotype Ontology, HP_0011766)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011766
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Genes

10 genes associated with the abnormality of the parathyroid morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CDC73 cell division cycle 73
CHD7 chromodomain helicase DNA binding protein 7
FLCN folliculin
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial
MEN1 multiple endocrine neoplasia I
NF1 neurofibromin 1
RET ret proto-oncogene
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
TBX1 T-box 1