methylmalonic aciduria and homocystinuria type cblC (Q18553420)
Jump to navigation
Jump to search
Human disease
- cobalamin C deficiency
- methylmalonic aciduria and homocystinuria, cblC type
- CblC defect
- Cobalamin C defect
- Methylmalonic Acidemia and Homocystinuria, Cblc Type
- Methylmalonic Aciduria and Homocystinuria, Vitamin B12-Responsive
- Methylmalonic aciduria with homocystinuria, type cblC
- Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblC
- Vitamin B12 Metabolic Defect With Combined Deficiency of Methylmalonyl-Coa Mutase and Homocysteine:Methyltetrahydrofolate Methyltransferase
- Methylmalonic acidemia with homocystinuria, type cblC
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | methylmalonic aciduria and homocystinuria type cblC |
Human disease |
|
Statements
1 reference
1 reference
7 references
1 reference
C142174
0 references
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference