| C1850600 |
Leigh Syndrome due to Mitochondrial Complex V Deficiency |
DO |
Leigh disease
|
3652 |
| C1850600 |
Leigh Syndrome due to Mitochondrial Complex V Deficiency |
MONDO |
Leigh syndrome
|
0009723 |
| C1850600 |
Leigh Syndrome due to Mitochondrial Complex V Deficiency |
MSH |
Leigh Syndrome due to Mitochondrial Complex V Deficiency
|
C564964 |
| C1850600 |
Leigh Syndrome due to Mitochondrial Complex V Deficiency |
OMIM |
LEIGH SYNDROME
|
256000 |
| C1850600 |
Leigh Syndrome due to Mitochondrial Complex V Deficiency |
OMIM |
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX II DEFICIENCY
|
256000 |
| C1850600 |
Leigh Syndrome due to Mitochondrial Complex V Deficiency |
OMIM |
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX III DEFICIENCY
|
256000 |
| C1850600 |
Leigh Syndrome due to Mitochondrial Complex V Deficiency |
OMIM |
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX V DEFICIENCY
|
256000 |
| C1850600 |
Leigh Syndrome due to Mitochondrial Complex V Deficiency |
OMIM |
NECROTIZING ENCEPHALOPATHY, INFANTILE SUBACUTE, OF LEIGH
|
256000 |
| C1850600 |
Leigh Syndrome due to Mitochondrial Complex V Deficiency |
ORDO |
Leigh syndrome
|
506 |