Fanconi Renotubular Syndrome 2 (FRTS2)

Alias:
Frts2
Fanconi Renotubular Syndrome, Type 2
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Fanconi Renotubular Syndrome 2, also known as frts2, is related to vitamin d-dependent rickets and vitamin d-dependent rickets type 2b, and has symptoms including muscle weakness An important gene associated with Fanconi Renotubular Syndrome 2 is SLC34A1 (Solute Carrier Family 34 Member 1), and among its related pathways/superpathways are Gene expression (Transcription) and Infectious disease. The drugs Temsirolimus and Benzocaine have been mentioned in the context of this disorder. Affiliated tissues include kidney and bone, and related phenotypes are osteopenia and short stature
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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9
19
3

Medical Symptom

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Description
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HPO Source Accession
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Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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