Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Preferred Name

TRANSFER RNA, MITOCHONDRIAL, LYSINE

Synonyms

tRNA-LYS, MITOCHONDRIAL

ID

http://purl.bioontology.org/ontology/OMIM/590060

altLabel

tRNA-LYS, MITOCHONDRIAL

PARKINSON DISEASE, MITOCHONDRIAL

DIABETES AND DEAFNESS, MATERNALLY INHERITED

CARDIOMYOPATHY AND DEAFNESS

MERRF/MELAS OVERLAP SYNDROME

MTTK

MERRF SYNDROME

PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MYOCLONUS

MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY SYNDROME

LEIGH SYNDROME

cui

C0023264

C4016621

C1538006

C0162672

C1838867

C0342289

C4016620

C4016622

C3151970

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/590060.0003

http://purl.bioontology.org/ontology/OMIM/590060.0004

http://purl.bioontology.org/ontology/OMIM/590060.0006

http://purl.bioontology.org/ontology/OMIM/590060.0005

http://purl.bioontology.org/ontology/OMIM/590060.0007

http://purl.bioontology.org/ontology/OMIM/590060.0001

http://purl.bioontology.org/ontology/OMIM/590060.0002

MIMTYPEMEANING

Gene with known sequence

notation

590060

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

TRANSFER RNA, MITOCHONDRIAL, LYSINE

tui

T028

T033

T047

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http://purl.bioontology.org/ontology/ICD10CM/G31.82 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/MESH/D017243 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C536246 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/ICD10CM/E88.42 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/MESH/D007888 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/LNC/LP31891-2 Logical Observation Identifier Names and Codes CUI
http://purl.bioontology.org/ontology/MESH/C564015 Medical Subject Headings CUI