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 1.3795

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 1.64

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 1.307

    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 0.1275

    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 0.600

    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 1.497

    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 1.158

    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 Leukodystrophy - paediatric


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.334

    Component of the following Super Panels:

  • Leukodystrophy_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 Hereditary Neuropathy - complex


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.45

    Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • 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 1.38

    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 0.278

    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 1.141

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