Complete deficiency of methylmalonyl-CoA mutase (Q104291): Difference between revisions
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Revision as of 10:09, 17 August 2026
This refers to complete deficiency of an enzyme that catalyzes the isomerization of methylmalonyl-CoA to succinyl-CoA and it is involved in key metabolic pathways. It requires a vitamin B12-derived prosthetic group, adenosylcobalamin, to function.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1741194419 |
||
| English | Complete deficiency of methylmalonyl-CoA mutase |
This refers to complete deficiency of an enzyme that catalyzes the isomerization of methylmalonyl-CoA to succinyl-CoA and it is involved in key metabolic pathways. It requires a vitamin B12-derived prosthetic group, adenosylcobalamin, to function. |
Statements
CID11:ID_1741194419
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dki-india-ID_1741194419
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Concluído
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