Intellectual Developmental Disorder, X-Linked 98 (XLID98)

Alias:
X-Linked Intellectual Disability, Cantagrel Type
Mental Retardation, X-Linked 98
Xlid98
Mrx98
Mental Retardation, X-Linked, Type 98
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Intellectual Developmental Disorder, X-Linked 98, also known as x-linked intellectual disability, cantagrel type, is related to non-syndromic x-linked intellectual disability 98, and has symptoms including muscle spasticity and seizures. An important gene associated with Intellectual Developmental Disorder, X-Linked 98 is NEXMIF (Neurite Extension And Migration Factor). Affiliated tissues include eye and brain, and related phenotypes are intellectual disability and short nose
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLD
XL
XLR
Newborn
<1/1000000
1
5
8

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
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