Sweeney-Cox Syndrome (SWCOS)

Alias:
Swcos
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Sweeney-Cox Syndrome, also known as swcos, is related to barber-say syndrome and acrofacial dysostosis, cincinnati type. An important gene associated with Sweeney-Cox Syndrome is TWIST1 (Twist Family BHLH Transcription Factor 1), and among its related pathways/superpathways are CKAP4 signaling pathway map and TGF-beta Signaling Pathways. Affiliated tissues include spleen and cerebellum, and related phenotypes are global developmental delay and hypertelorism
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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17
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Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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