loading...| Preferred Name |
COMPLEX I, SUBUNIT ND5 |
| Synonyms |
MELAS SYNDROME |
| ID |
http://purl.bioontology.org/ontology/OMIM/516005 |
| altLabel |
MELAS SYNDROME MTND5 MERRF SYNDROME NADH-UBIQUINONE OXIDOREDUCTASE, SUBUNIT ND5 NADH DEHYDROGENASE, SUBUNIT 5 LEBER OPTIC ATROPHY PARKINSON DISEASE 6, MODIFIER OF LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY |
| cui |
C0162672 C1537994 C1838951 C4016598 C0162671 C0917796 |
| Has allelic variant |
http://purl.bioontology.org/ontology/OMIM/516005.0008 http://purl.bioontology.org/ontology/OMIM/516005.0009 http://purl.bioontology.org/ontology/OMIM/516005.0004 http://purl.bioontology.org/ontology/OMIM/516005.0011 http://purl.bioontology.org/ontology/OMIM/516005.0005 http://purl.bioontology.org/ontology/OMIM/516005.0006 http://purl.bioontology.org/ontology/OMIM/516005.0001 http://purl.bioontology.org/ontology/OMIM/516005.0003 http://purl.bioontology.org/ontology/OMIM/516005.0002 |
| MIMTYPEMEANING |
Gene with known sequence |
| notation |
516005 |
| OMIM Entry Type |
1 |
| OMIM MimType Value |
star |
| prefLabel |
COMPLEX I, SUBUNIT ND5 |
| tui |
T028 T033 T047 |