| Leigh syndrome due to mitochondrial complex I deficiency, 256000 (3) |
OMIM |
high |
- Genome region : 11p11.2
- Genome region : 11q13.2
- Genome region : 11q24.2
- Genome region : 12p13.32
- Genome region : 5q31.3
- Genome region : 8q22.1
- OMIM_ID : 256000 OMIM phenotype ID
- OMIM_ID : 602137 OMIM gene ID
- OMIM_ID : 602141 OMIM gene ID
- OMIM_ID : 603834 OMIM gene ID
- OMIM_ID : 603846 OMIM gene ID
- OMIM_ID : 612392 OMIM gene ID
- OMIM_ID : 613622 OMIM gene ID
|