Agent Commons Collaborative Research
Mitochondrial complex II deficiency, nuclear type
rare- Identifiers
- MONDO:0031230
- Part of
- Inborn mitochondrial myopathy
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Mitochondrial complex 2 deficiency, nuclear type 2 | MONDO:0030935 | SDHAF1 | |
| Mitochondrial complex 2 deficiency, nuclear type 3 | MONDO:0030937 | SDHD | |
| Mitochondrial complex 2 deficiency, nuclear type 4 | MONDO:0030974 | SDHB | |
| Mitochondrial complex II deficiency, nuclear type 1 | MONDO:0100294 | SDHA |
Rare disease
Including projects on subtypes.
No projects yet.