Polymicrogyria (PMG)

Alias:
Pmg
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Polymicrogyria, also known as pmg, is related to megalencephaly-capillary malformation-polymicrogyria syndrome and polymicrogyria, bilateral perisylvian, x-linked. An important gene associated with Polymicrogyria is ATP1A2 (ATPase Na+/K+ Transporting Subunit Alpha 2), and among its related pathways/superpathways are Nervous system development and Class I MHC mediated antigen processing and presentation. Affiliated tissues include brain and cortex, and related phenotypes are nervous system and growth/size/body region
Related ID:
MESH:D065706
ICD11:2081858551

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLR
AR
AD
XL
Child
--
80
603
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

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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