Mitochondrial Complex I Deficiency, Nuclear Type 37 (MC1DN37)

Alias:
Mitochondrial Complex 1 Deficiency, Nuclear Type 37
Mc1dn37
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Mitochondrial Complex I Deficiency, Nuclear Type 37, is also known as mitochondrial complex 1 deficiency, nuclear type 37. An important gene associated with Mitochondrial Complex I Deficiency, Nuclear Type 37 is NDUFA8 (NADH:Ubiquinone Oxidoreductase Subunit A8). Affiliated tissues include liver and skeletal muscle, and related phenotypes are failure to thrive and tetraplegia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
4
2

Medical Symptom

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Categorization
Description
HPO Frequency
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No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

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MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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