Variants
Genes
Phenotypes
Pricing
Sign InSign Up

Combined oxidative phosphorylation deficiency

Your Results

Sign In

Description

A mitochondrial oxidative phosphorylation disorder in which multiple mitochondrial respiratory chain complexes.

MONDO

  • Mode of Inheritance

    VARIANTS

    117

    SEE THE VARIANTS →

    Genes

    • AARS2
    • AIFM1
    • ATP5F1A
    • C1QBP
    • CARS2
    • EARS2
    • ELAC2
    • FARS2
    • GFM1
    • GTPBP3
    • LYRM4
    • MARS2
    • MICOS13
    • MIPEP
    • MRPL3
    • MRPL44
    • MRPS16
    • MRPS2
    • MRPS22
    • MRPS34
    • MRPS7
    • MTFMT
    • MTO1
    • MTRFR
    • NARS2
    • PNPT1
    • RMND1
    • SFXN4
    • SLC25A26
    • TARS2
    • TRIT1
    • TRMT10C
    • TRMT5
    • TSFM
    • TUFM
    • TXN2
    • VARS2

    External Links

    • OMIM
    • Orphanet
    • HPO
    • Medgen

      C4540031

    © 2024 Biocodify. All rights reserved.

    TwitterTwitter

    Product

    HomePricingDashboard

    DNA

    VariantsGenesPhenotypes

    Stay up to date

    The latest news and updates from Biocodify, sent to your inbox.