Delpire-Mcneill Syndrome (DELMNES)

Alias:
Delmnes
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Delpire-Mcneill Syndrome, is also known as delmnes. An important gene associated with Delpire-Mcneill Syndrome is SLC12A2 (Solute Carrier Family 12 Member 2). Affiliated tissues include trachea and respiratory system-trachea, and related phenotypes are global developmental delay and autistic behavior
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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
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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