Intellectual Developmental Disorder, X-Linked, Syndromic, Claes-Jensen Type (MRXSCJ)

Alias:
Mental Retardation, X-Linked, Syndromic, Claes-Jensen Type
Mental Retardation, X-Linked, Syndromic, Jarid1c-Related
Mrxscj
Mrxsj
Intellectual Developmental Disorder, X-Linked Syndromic, Claes-Jensen Type
Syndromic X-Linked Intellectual Disability Claes-Jensen Type
Kdm5c-Related Syndromic X-Linked Intellectual Disability
Kdm5c-Related X-Linked Syndromic Intellectual Disability
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Intellectual Developmental Disorder, X-Linked, Syndromic, Claes-Jensen Type, also known as mental retardation, x-linked, syndromic, claes-jensen type, is related to syndromic x-linked intellectual disability claes-jensen type and plasma cell neoplasm. An important gene associated with Intellectual Developmental Disorder, X-Linked, Syndromic, Claes-Jensen Type is KDM5C (Lysine Demethylase 5C). Affiliated tissues include eye and tongue, and related phenotypes are delayed speech and language development and intellectual disability, severe
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XL
XLD
Child
<1/1000000
1
10
17

Medical Symptom

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

Gene & Mutation

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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

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PMID
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Year
IF
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