Mitochondrial Complex I Deficiency, Nuclear Type 36 (MC1DN36)

Alias:
Mitochondrial Complex 1 Deficiency, Nuclear Type 36
Mc1dn36
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Mitochondrial Complex I Deficiency, Nuclear Type 36, also known as mitochondrial complex 1 deficiency, nuclear type 36, is related to mitochondrial disease. An important gene associated with Mitochondrial Complex I Deficiency, Nuclear Type 36 is NDUFC2 (NADH:Ubiquinone Oxidoreductase Subunit C2). Affiliated tissues include eye and liver, and related phenotypes are global developmental delay and increased serum lactate
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Basic Information

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

Medical Symptom

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Categorization
Description
HPO Frequency
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HPO Source Accession
No data available

Gene & Mutation

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Mutations
No data available

Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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IF
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