Cornelia De Lange Syndrome 4 with or Without Midline Brain Defects (CDLS4)

Alias:
Cornelia De Lange Syndrome 4
Cdls4
Cornelia De Lange Syndrome, Type 4
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cornelia De Lange Syndrome 4 with or Without Midline Brain Defects, also known as cornelia de lange syndrome 4, is related to trichorhinophalangeal syndrome and trichorhinophalangeal syndrome, type i. An important gene associated with Cornelia De Lange Syndrome 4 with or Without Midline Brain Defects is RAD21 (RAD21 Cohesin Complex Component), and among its related pathways/superpathways are Cell Cycle, Mitotic and EML4 and NUDC in mitotic spindle formation. Affiliated tissues include brain and heart, and related phenotypes are cleft palate and hemivertebrae
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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16
80
12

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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References Literature

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