Intellectual Developmental Disorder, X-Linked 19 (XLID19)

Alias:
Xlid19
Mrx19
Mental Retardation, X-Linked, Type 19
Intellectual Disability, X-Linked 19
Mrx31
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Intellectual Developmental Disorder, X-Linked 19, also known as xlid19, is related to chromosome xp11.22 duplication syndrome and coffin-lowry syndrome. An important gene associated with Intellectual Developmental Disorder, X-Linked 19 is RPS6KA3 (Ribosomal Protein S6 Kinase A3). Affiliated tissues include brain, and related phenotypes are intellectual disability, mild and intellectual disability
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XL
XLR
Unknown
--
1
5
21

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!
Wechat
Comparison
Al agent
Tutorials
Back to top