Fanconi Renotubular Syndrome 5 (FRTS5)

Alias:
Fanconi Renotubular Syndrome, Acadian Variant
Frts5
Acadian-Variant Fanconi Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Fanconi Renotubular Syndrome 5, is also known as fanconi renotubular syndrome, acadian variant. An important gene associated with Fanconi Renotubular Syndrome 5 is NDUFAF6 (NADH:Ubiquinone Oxidoreductase Complex Assembly Factor 6). Affiliated tissues include kidney and lung, and related phenotypes are genu valgum and tubulointerstitial fibrosis
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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
3
3

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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