multiple carpal ossification centers Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A delay in the process of formation and maturation of the epiphysis of one or more long bones. (Human Phenotype Ontology, HP_0006067)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006067
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Genes

2 genes associated with the multiple carpal ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
FLNB filamin B, beta