Entry Search - 161700 500017 516000 516001 516002 516003 516005 516006 516030 516040 516050 516060 590045 590050 590060 590095 590105

Search: '161700 500017 516000 516001 516002 516003 516005 516006 516030 516040 516050 516060 590045 590050 590060 590095 590105 (Search in: MIM number)'

Results: 17 entries.

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161700. NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT
Matching terms: 161700
► Links

Links
Clinical Resources Clinical Trials Gene Reviews	Animal Models OMIA

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# 500017. LEIGH SYNDROME, MITOCHONDRIAL; MILS
Matching terms: 500017
► ICD+ ► Links

Links
Testing EuroGentest	Clinical Resources Clinical Trials EuroGentest Gene Reviews OrphaNet

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ICD+
SNOMEDCT: 717052002 ORPHA: 255210

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* 516000. COMPLEX I, SUBUNIT ND1; MTND1
MITOCHONDRIAL COMPLEX I DEFICIENCY, MITOCHONDRIAL TYPE 3, INCLUDED; MC1DM3, INCLUDED
Matching terms: 516000
► ICD+ ► Links

Links
Testing GTR	Genome Ensembl MITOMAP NCBI Genome Viewer UCSC Genome Browser	DNA Ensembl UCSC Genome Browser	Protein Human Protein Atlas NCBI Protein UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG MARRVEL Monarch NCBI Gene	Clinical Resources ClinGen Validity MedlinePlus Genetics GTR	Variation ClinVar DECIPHER gnomAD GWAS Central HGMD NHLBI EVS PharmGKB	Animal Models Alliance Genome FlyBase IMPC MARRVEL MGI Mouse Gene MMRRC NCBI Orthologs OrthoDB	Cell Lines Coriell	Cellular Pathways KEGG Reactome

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ICD+
SNOMEDCT: 26929004, 39925003, 49049000, 51178009, 58610003 ICD10CM: E88.41, G20, G20.A1, G30, G30.9, H47.22 ICD9CM: 331.0, 332, 332.0, 798.0

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* 516001. COMPLEX I, SUBUNIT ND2; MTND2
Matching terms: 516001
► ICD+ ► Links

Links
Testing GTR	Genome Ensembl MITOMAP NCBI Genome Viewer UCSC Genome Browser	DNA Ensembl UCSC Genome Browser	Protein Human Protein Atlas NCBI Protein UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG MARRVEL Monarch NCBI Gene	Clinical Resources ClinGen Validity GTR	Variation ClinVar gnomAD GWAS Central HGMD NHLBI EVS PharmGKB	Animal Models Alliance Genome FlyBase IMPC MARRVEL MGI Mouse Gene MMRRC NCBI Orthologs OrthoDB	Cellular Pathways KEGG Reactome

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ICD+
SNOMEDCT: 237988006, 58610003 ICD10CM: H47.22

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* 516002. COMPLEX I, SUBUNIT ND3; MTND3
Matching terms: 516002
► Links

Links
Testing GTR	Genome Ensembl MITOMAP NCBI Genome Viewer UCSC Genome Browser	DNA Ensembl UCSC Genome Browser	Protein Human Protein Atlas NCBI Protein UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG MARRVEL Monarch NCBI Gene	Clinical Resources ClinGen Validity GTR	Variation ClinVar gnomAD GWAS Central HGMD NHLBI EVS PharmGKB	Animal Models Alliance Genome FlyBase IMPC MARRVEL MGI Mouse Gene MMRRC NCBI Orthologs OrthoDB	Cellular Pathways KEGG Reactome

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* 516003. COMPLEX I, SUBUNIT ND4; MTND4
Matching terms: 516003
► ICD+ ► Links

Links
Testing GTR	Genome Ensembl MITOMAP NCBI Genome Viewer UCSC Genome Browser	DNA Ensembl UCSC Genome Browser	Protein Human Protein Atlas NCBI Protein UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG MARRVEL Monarch NCBI Gene	Clinical Resources ClinGen Validity MedlinePlus Genetics GTR	Variation ClinVar gnomAD GWAS Central HGMD NHLBI EVS PharmGKB	Animal Models Alliance Genome FlyBase IMPC MARRVEL MGI Mouse Gene MMRRC NCBI Orthologs OrthoDB	Cell Lines Coriell	Cellular Pathways KEGG Reactome

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ICD+
SNOMEDCT: 237988006, 39925003, 58610003 ICD10CM: E88.41, H47.22

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* 516005. COMPLEX I, SUBUNIT ND5; MTND5
Matching terms: 516005
► ICD+ ► Links

Links
Testing GTR	Genome Ensembl MITOMAP NCBI Genome Viewer UCSC Genome Browser	DNA Ensembl UCSC Genome Browser	Protein Human Protein Atlas NCBI Protein UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG MARRVEL Monarch NCBI Gene	Clinical Resources ClinGen Validity MedlinePlus Genetics GTR	Variation ClinVar DECIPHER gnomAD GWAS Central HGMD NHLBI EVS PharmGKB	Animal Models Alliance Genome FlyBase IMPC MARRVEL MGI Mouse Gene MMRRC NCBI Orthologs OrthoDB	Cellular Pathways KEGG Reactome

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ICD+
SNOMEDCT: 230426003, 39925003, 58610003 ICD10CM: E88.41, E88.42, H47.22

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* 516006. COMPLEX I, SUBUNIT ND6; MTND6
Matching terms: 516006
► ICD+ ► Links

Links
Testing GTR	Genome Ensembl MITOMAP NCBI Genome Viewer UCSC Genome Browser	DNA Ensembl UCSC Genome Browser	Protein Human Protein Atlas NCBI Protein UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG MARRVEL Monarch NCBI Gene	Clinical Resources ClinGen Validity MedlinePlus Genetics GTR	Variation ClinVar gnomAD GWAS Central HGMD NHLBI EVS PharmGKB	Animal Models Alliance Genome IMPC MARRVEL MGI Mouse Gene MMRRC NCBI Orthologs OrthoDB	Cellular Pathways KEGG Reactome

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ICD+
SNOMEDCT: 39925003, 58610003, 89439007 ICD10CM: E88.41, H47.22

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* 516030. COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT I; MTCO1
Matching terms: 516030
► ICD+ ► Links

Links
Testing GTR	Genome Ensembl MITOMAP NCBI Genome Viewer UCSC Genome Browser	DNA Ensembl UCSC Genome Browser	Protein Human Protein Atlas NCBI Protein UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG MARRVEL Monarch NCBI Gene	Clinical Resources ClinGen Validity GTR	Variation ClinVar DECIPHER gnomAD GWAS Central HGMD NHLBI EVS PharmGKB	Animal Models Alliance Genome FlyBase IMPC MARRVEL MGI Mouse Gene MMRRC NCBI Orthologs OrthoDB	Cellular Pathways KEGG Reactome

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ICD+
SNOMEDCT: 58610003, 67434000 ICD10CM: H47.22

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10:

* 516040. COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT II; MTCO2
Matching terms: 516040
► ICD+ ► Links

Links
Testing GTR	Genome Ensembl MITOMAP NCBI Genome Viewer UCSC Genome Browser	DNA Ensembl UCSC Genome Browser	Protein Human Protein Atlas NCBI Protein UniProt	Gene Info BioGPS Ensembl GeneCards Gene Ontology KEGG MARRVEL Monarch NCBI Gene	Clinical Resources ClinGen Validity GTR	Variation ClinVar DECIPHER gnomAD GWAS Central HGMD NHLBI EVS PharmGKB	Animal Models Alliance Genome FlyBase IMPC MARRVEL MGI Mouse Gene MMRRC NCBI Orthologs OrthoDB	Cellular Pathways KEGG Reactome

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ICD+
SNOMEDCT: 67434000

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Search: 161700 500017 516000 516001 516002 516003 516005 516006 516030 516040 516050 516060 590045 590050 590060 590095 590105 (Search in: MIM number)

Results: 17 entries.

161700. NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT
Matching terms: 161700

# 500017. LEIGH SYNDROME, MITOCHONDRIAL; MILS
Matching terms: 500017

* 516000. COMPLEX I, SUBUNIT ND1; MTND1
MITOCHONDRIAL COMPLEX I DEFICIENCY, MITOCHONDRIAL TYPE 3, INCLUDED; MC1DM3, INCLUDED
Matching terms: 516000

* 516001. COMPLEX I, SUBUNIT ND2; MTND2
Matching terms: 516001

* 516002. COMPLEX I, SUBUNIT ND3; MTND3
Matching terms: 516002

* 516003. COMPLEX I, SUBUNIT ND4; MTND4
Matching terms: 516003

* 516005. COMPLEX I, SUBUNIT ND5; MTND5
Matching terms: 516005

* 516006. COMPLEX I, SUBUNIT ND6; MTND6
Matching terms: 516006

* 516030. COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT I; MTCO1
Matching terms: 516030

10:

* 516040. COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT II; MTCO2
Matching terms: 516040

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