Disease #02120 (MAHCC (aciduria, methylmalonic, and homocystinuria, cblC type (MAHCC)), OMIM:277400)
| Official abbreviation |
MAHCC |
| Name |
aciduria, methylmalonic, and homocystinuria, cblC type (MAHCC) |
| OMIM ID |
277400 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 2 genes |
MMACHC, PRDX1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-07-09 16:30:16 +02:00 (CEST) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|