| Preferred Name |
COMPLEX I, SUBUNIT ND1 |
| Synonyms |
MITOCHONDRIAL COMPLEX I DEFICIENCY |
| ID |
http://purl.bioontology.org/ontology/OMIM/516000 |
| altLabel |
MITOCHONDRIAL COMPLEX I DEFICIENCY DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL ALZHEIMER DISEASE NADH DEHYDROGENASE, SUBUNIT 1 NADH-UBIQUINONE OXIDOREDUCTASE, SUBUNIT ND1 COLORECTAL CANCER LEBER OPTIC ATROPHY AND DYSTONIA MELAS SYNDROME MTND1 PARKINSON DISEASE DYSTONIA, ADULT-ONSET NADH-DEHYDROGENASE SUBUNIT 1, MITOCHONDRIAL, MUTATION IN SUDDEN INFANT DEATH SYNDROME LEBER OPTIC ATROPHY |
| cui |
C0038644 C1838979 C1527249 C1537989 C0162671 C0917796 C4017625 C0002395 C0752197 C0030567 C1839040 C3151897 |
| Has allelic variant |
http://purl.bioontology.org/ontology/OMIM/516000.0006 http://purl.bioontology.org/ontology/OMIM/516000.0008 http://purl.bioontology.org/ontology/OMIM/516000.0007 http://purl.bioontology.org/ontology/OMIM/516000.0015 http://purl.bioontology.org/ontology/OMIM/516000.0003 http://purl.bioontology.org/ontology/OMIM/516000.0012 http://purl.bioontology.org/ontology/OMIM/516000.0010 http://purl.bioontology.org/ontology/OMIM/516000.0011 http://purl.bioontology.org/ontology/OMIM/516000.0004 http://purl.bioontology.org/ontology/OMIM/516000.0005 http://purl.bioontology.org/ontology/OMIM/516000.0016 http://purl.bioontology.org/ontology/OMIM/516000.0009 http://purl.bioontology.org/ontology/OMIM/516000.0001 http://purl.bioontology.org/ontology/OMIM/516000.0002 |
| MIMTYPEMEANING |
Gene with known sequence |
| notation |
516000 |
| OMIM Entry Type |
1 |
| OMIM MimType Value |
star |
| prefLabel |
COMPLEX I, SUBUNIT ND1 |
| tui |
T191 T028 T033 T047 |