Online Mendelian Inheritance in Man

Last uploaded: January 31, 2024
Preferred Name

COMPLEX I, SUBUNIT ND2

Synonyms

MTND2

ID

http://purl.bioontology.org/ontology/OMIM/516001

altLabel

MTND2

NADH DEHYDROGENASE, SUBUNIT 2

LEBER OPTIC ATROPHY

NADH-UBIQUINONE OXIDOREDUCTASE, SUBUNIT ND2

MITOCHONDRIAL COMPLEX I DEFICIENCY

LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY

cui

C1838951

C1537990

C0917796

C1838979

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/516001.0006

http://purl.bioontology.org/ontology/OMIM/516001.0002

http://purl.bioontology.org/ontology/OMIM/516001.0004

http://purl.bioontology.org/ontology/OMIM/516001.0001

http://purl.bioontology.org/ontology/OMIM/516001.0003

http://purl.bioontology.org/ontology/OMIM/516001.0005

MIMTYPEMEANING

Gene with known sequence

notation

516001

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

COMPLEX I, SUBUNIT ND2

tui

T047

T028

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