Chiari Malformation Type I (CM1)

Alias:
Arnold-Chiari Malformation Type I
Arnold-Chiari Malformation Type 1
Chiari Malformation Type 1
Arnold-Chiari Malformation, Type I
Arnold-Chiari Obstruction Type I
Malformation, Chiari, Type I
Chiari Type 1 Malformation
Cm1
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Chiari Malformation Type I, also known as arnold-chiari malformation type i, is related to chiari malformation type ii and craniosynostosis-hydrocephalus-arnold-chiari malformation type i-radioulnar synostosis syndrome, and has symptoms including neck pain, dizziness and facial pain. An important gene associated with Chiari Malformation Type I is DKK1 (Dickkopf WNT Signaling Pathway Inhibitor 1). Affiliated tissues include spinal cord and tonsil, and related phenotypes are chiari type i malformation and headache
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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1
14
34

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Score
Mutations
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Related Drugs

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No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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