cystathioninemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased concentration of cystathionine in the blood. (Human Phenotype Ontology, HP_0003286)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003286
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
LMBRD1 LMBR1 domain containing 1
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria