Abnormality of mitochondrial metabolism (Phenotype)

Synonyms:Mitochondrial dysfunction
Id:HP:0003287
Description:A functional anomaly of mitochondria.
Results found

Linked to

 

Label

Description

 

Gene

ENSG00000040531 - cystinosin, lysosomal cystine transporter

Gene

ENSG00000198804 - mitochondrially encoded cytochrome c oxidase I [Source:HGNC Symbol;Acc:HGNC:7419]

Gene

ENSG00000141385 - AFG3 like matrix AAA peptidase subunit 2

Gene

ENSG00000056998 - glycogenin 2

Gene

ENSG00000139438 - family with sequence similarity 222 member A

Gene

ENSG00000278533 - osteoclast associated Ig-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]

Gene

ENSG00000138271 - G protein-coupled receptor 87

Gene

ENSG00000006744 - elaC ribonuclease Z 2

Gene

ENSG00000273607 - coiled-coil-helix-coiled-coil-helix domain containing 10 [Source:HGNC Symbol;Acc:HGNC:15559]

Gene

ENSG00000168291 - pyruvate dehydrogenase E1 subunit beta

  • Gene

    ENSG00000040531 - cystinosin, lysosomal cystine transporter


  • Gene

    ENSG00000198804 - mitochondrially encoded cytochrome c oxidase I [Source:HGNC Symbol;Acc:HGNC:7419]


  • Gene

    ENSG00000141385 - AFG3 like matrix AAA peptidase subunit 2


  • Gene

    ENSG00000056998 - glycogenin 2


  • Gene

    ENSG00000139438 - family with sequence similarity 222 member A


  • Gene

    ENSG00000278533 - osteoclast associated Ig-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]


  • Gene

    ENSG00000138271 - G protein-coupled receptor 87


  • Gene

    ENSG00000006744 - elaC ribonuclease Z 2


  • Gene

    ENSG00000273607 - coiled-coil-helix-coiled-coil-helix domain containing 10 [Source:HGNC Symbol;Acc:HGNC:15559]


  • Gene

    ENSG00000168291 - pyruvate dehydrogenase E1 subunit beta

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