Intellectual Developmental Disorder, X-Linked 99, Syndromic, Female-Restricted (MRXS99F)

Alias:
Mental Retardation, X-Linked 99, Syndromic, Female-Restricted
Mrxs99f
Intellectual Disability, X-Linked 99, Syndromic, Female-Restricted
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Intellectual Developmental Disorder, X-Linked 99, Syndromic, Female-Restricted, also known as mental retardation, x-linked 99, syndromic, female-restricted, is related to female-restricted syndromic x-linked intellectual disability 99. An important gene associated with Intellectual Developmental Disorder, X-Linked 99, Syndromic, Female-Restricted is USP9X (Ubiquitin Specific Peptidase 9 X-Linked). Affiliated tissues include brain and heart, and related phenotypes are global developmental delay and ventriculomegaly
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XL
XLR
Unknown
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1
8
3

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

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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
Journal
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IF
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