Robinow Syndrome, Autosomal Dominant 3 (DRS3)

Alias:
Autosomal Dominant Robinow Syndrome 3
Drs3
Robinow, Autosomal Dominant Syndrome, Type 3
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Robinow Syndrome, Autosomal Dominant 3, also known as autosomal dominant robinow syndrome 3, is related to omodysplasia and autosomal dominant robinow syndrome. An important gene associated with Robinow Syndrome, Autosomal Dominant 3 is DVL3 (Dishevelled Segment Polarity Protein 3), and among its related pathways/superpathways are Transcription Androgen Receptor nuclear signaling and mTOR Signaling. Affiliated tissues include heart and tongue, and related phenotypes are gingival overgrowth and wide nasal bridge
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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8
52
1

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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