Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Preferred Name

COMPLEX I, SUBUNIT ND3

Synonyms

MITOCHONDRIAL COMPLEX I DEFICIENCY

ID

http://purl.bioontology.org/ontology/OMIM/516002

altLabel

MITOCHONDRIAL COMPLEX I DEFICIENCY

LEBER OPTIC ATROPHY AND DYSTONIA

NADH DEHYDROGENASE, SUBUNIT 3

PARKINSON DISEASE, RESISTANCE TO

MTND3

NADH-UBIQUINONE OXIDOREDUCTASE, SUBUNIT ND3

LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY

cui

C1838979

C1838951

C1537991

C1839040

C4016597

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/516002.0002

http://purl.bioontology.org/ontology/OMIM/516002.0004

http://purl.bioontology.org/ontology/OMIM/516002.0003

http://purl.bioontology.org/ontology/OMIM/516002.0001

MIMTYPEMEANING

Gene with known sequence

notation

516002

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

COMPLEX I, SUBUNIT ND3

tui

T028

T033

T047

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http://purl.bioontology.org/ontology/MESH/C564021 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C537475 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C536024 Medical Subject Headings CUI