MT-ND4

mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4
OMIM: 516003, ClinGen, DECIPHER

12 panels

Panel Reviews Mode of inheritance Details
12 panels

Green MT-ND4 in Mendeliome


Version 1.4540

1 review MITOCHONDRIAL
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Mitochondrial disease (MONDO:0044970), MT-ND4-related
Tags
  • mtDNA

Green MT-ND4 in Optic Atrophy


Level 2: Ophthalmological disorders
Version 1.68

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • 1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    • Expert list
    Phenotypes
    • Mitochondrial disease (MONDO:0044970), MT-ND4-related
    Tags
    • mtDNA

    Green MT-ND4 in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.384

    Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    • Expert list
    Phenotypes
    • Mitochondrial disease (MONDO:0044970), MT-ND4-related
    Tags
    • mtDNA

    Green MT-ND4 in Mitochondrial disease


    Level 2: Metabolic disorders
    Version 1.16

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • 1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Mitochondrial disease (MONDO:0044970), MT-ND4-related
    Tags
    • mtDNA

    Green MT-ND4 in Regression


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.607

    1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    • Expert list
    Phenotypes
    • Mitochondrial disease (MONDO:0044970), MT-ND4-related
    Tags
    • mtDNA

    Green MT-ND4 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.699

    1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    • Expert list
    Phenotypes
    • Mitochondrial disease (MONDO:0044970), MT-ND4-related
    Tags
    • mtDNA

    Green MT-ND4 in Ataxia


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.192

    Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • 1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    • Expert list
    Phenotypes
    • Mitochondrial disease (MONDO:0044970), MT-ND4-related
    Tags
    • mtDNA

    Green MT-ND4 in Leukodystrophy


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.392

    Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    • Expert list
    Phenotypes
    • Mitochondrial disease (MONDO:0044970), MT-ND4-related
    Tags
    • mtDNA

    Green MT-ND4 in Hereditary Neuropathy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.186

    Component of the following Super Panels:

  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • 1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    • Expert list
    Phenotypes
    • Mitochondrial disease (MONDO:0044970), MT-ND4-related
    Tags
    • mtDNA

    Green MT-ND4 in Stroke


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.46

    1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    • Expert list
    Phenotypes
    • Mitochondrial disease (MONDO:0044970), MT-ND4-related
    Tags
    • mtDNA

    Red MT-ND4 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.280

    0 reviews MITOCHONDRIAL
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Leber hereditary optic neuropathy

    Red MT-ND4 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.147

    0 reviews MITOCHONDRIAL
    Sources
    • BabySeq Category C gene
    • Expert Review Red
    Phenotypes
    • Leber hereditary optic neuropathy