Currarino Syndrome (CURRAS)

Alias:
Currarino Triad
Curras
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Currarino Syndrome, also known as currarino triad, is related to holoprosencephaly and sacral defect with anterior meningocele, and has symptoms including chronic constipation An important gene associated with Currarino Syndrome is MNX1 (Motor Neuron And Pancreas Homeobox 1). Affiliated tissues include spinal cord and bone, and related phenotypes are aplasia/hypoplasia of the sacrum and sacrococcygeal teratoma
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
All ages
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29
126
23

Medical Symptom

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Description
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HPO Source Accession
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Gene & Mutation

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Related Drugs

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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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