Mitochondrial Complex I Deficiency, Nuclear Type 26 (MC1DN26)

Alias:
Mc1dn26
Mitochondrial Complex 1 Deficiency, Nuclear Type 26
Nuclear Type Mitochondrial Complex I Deficiency 26
Mi Complex I Deficiency, Nuclear Type 26
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Mitochondrial Complex I Deficiency, Nuclear Type 26, is also known as mc1dn26. An important gene associated with Mitochondrial Complex I Deficiency, Nuclear Type 26 is NDUFA9 (NADH:Ubiquinone Oxidoreductase Subunit A9). Affiliated tissues include liver, and related phenotypes are respiratory insufficiency and hearing impairment
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
3
2

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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