| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A decreased concentration of methionine in the blood. (Human Phenotype Ontology, HP_0003658) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0003658 |
| Similar Terms | |
| Downloads & Tools |
4 genes associated with the hypomethioninemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| MMACHC | methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria |
| MMADHC | methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria |
| MTR | 5-methyltetrahydrofolate-homocysteine methyltransferase |
| MTRR | 5-methyltetrahydrofolate-homocysteine methyltransferase reductase |
