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Chromosome Xq25 Duplication Syndrome (DUP)

Alias:
Xq25 Microduplication Syndrome
Xq25 Duplication Syndrome
Xq25 Microtriplication
Dup
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Chromosome Xq25 Duplication Syndrome, is also known as xq25 microduplication syndrome. An important gene associated with Chromosome Xq25 Duplication Syndrome is DUPXQ25 (Xq25 Duplication Syndrome). Affiliated tissues include brain, and related phenotypes are seizure and global developmental delay
Related ID：
MALACARDS：CHR722
OMIM：300979

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLD
XL
XLR
Infant
<1/1000000
1
8
4
CHR722

Medical Symptom

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

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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