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Meningocele

Alias:
Congenital Meningocele
Spinal Meningocele
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Meningocele, also known as congenital meningocele, is related to lateral meningocele syndrome and sacral defect with anterior meningocele. An important gene associated with Meningocele is NOTCH3 (Notch Receptor 3), and among its related pathways/superpathways is Folate-alcohol and cancer pathway hypotheses. Affiliated tissues include spinal cord and bone marrow, and related phenotypes are nervous system and limbs/digits/tail
Related ID：
MALACARDS：MNN007

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Newborn
--
20
167
--
MNN007

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
No Data Found!
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