Microphthalmia, Syndromic 11 (MCOPS11)

Alias:
Mcops11
Microphthalmia with Corpus Callosum Agenesis and Orofacial Clefting
Microphthalmia, Syndromic, Type 11
Microphthalmia, Syndromic, 11
Syndromic Microphthalmia 11
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Microphthalmia, Syndromic 11, is also known as mcops11. An important gene associated with Microphthalmia, Syndromic 11 is VAX1 (Ventral Anterior Homeobox 1). Affiliated tissues include pineal and eye, and related phenotypes are agenesis of corpus callosum and global developmental delay
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
7
1

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

Title
PMID
Journal
Year
IF
No Data Found!
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