Online Mendelian Inheritance in Man

Last uploaded: January 31, 2024
Preferred Name

COMPLEX I, SUBUNIT ND1

Synonyms

SUDDEN INFANT DEATH SYNDROME

ID

http://purl.bioontology.org/ontology/OMIM/516000

altLabel

SUDDEN INFANT DEATH SYNDROME

NADH DEHYDROGENASE, SUBUNIT 1

MELAS SYNDROME

ALZHEIMER DISEASE

PARKINSON DISEASE

COLORECTAL CANCER

DYSTONIA, ADULT-ONSET

MC1DM3

MTND1

MITOCHONDRIAL COMPLEX I DEFICIENCY, MITOCHONDRIAL TYPE 3

LEBER OPTIC ATROPHY AND DYSTONIA

NADH-DEHYDROGENASE SUBUNIT 1, MITOCHONDRIAL, MUTATION IN

DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL

LEBER OPTIC ATROPHY

NADH-UBIQUINONE OXIDOREDUCTASE, SUBUNIT ND1

cui

C0030567

C1839040

C0009402

C0162671

C0038644

C3151897

C4017625

C4722144

C0752197

C1537989

C0917796

C0002395

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/516000.0004

http://purl.bioontology.org/ontology/OMIM/516000.0007

http://purl.bioontology.org/ontology/OMIM/516000.0009

http://purl.bioontology.org/ontology/OMIM/516000.0006

http://purl.bioontology.org/ontology/OMIM/516000.0005

http://purl.bioontology.org/ontology/OMIM/516000.0002

http://purl.bioontology.org/ontology/OMIM/516000.0001

http://purl.bioontology.org/ontology/OMIM/516000.0003

http://purl.bioontology.org/ontology/OMIM/516000.0008

http://purl.bioontology.org/ontology/OMIM/516000.0014

http://purl.bioontology.org/ontology/OMIM/516000.0013

http://purl.bioontology.org/ontology/OMIM/516000.0010

http://purl.bioontology.org/ontology/OMIM/516000.0011

http://purl.bioontology.org/ontology/OMIM/516000.0016

http://purl.bioontology.org/ontology/OMIM/516000.0015

http://purl.bioontology.org/ontology/OMIM/516000.0012

MIMTYPEMEANING

Gene with known sequence

notation

516000

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

COMPLEX I, SUBUNIT ND1

tui

T047

T033

T191

T028

Delete Subject Author Type Created
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Create mapping

Delete Mapping To Ontology Source
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