Disease #02119 (MAHCF (aciduria, methylmalonic, and homocystinuria, cblF type (MAHCF)), OMIM:277380)
| Official abbreviation |
MAHCF |
| Name |
aciduria, methylmalonic, and homocystinuria, cblF type (MAHCF) |
| OMIM ID |
277380 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
LMBRD1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-09-06 13:59:34 +02:00 (CEST) |
Individuals
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