Lateral Meningocele Syndrome (LMNS)

Alias:
Lehman Syndrome
Lms
Lmns
Meningocele, Lateral Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Lateral Meningocele Syndrome, also known as lehman syndrome, is related to meningocele and cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1. An important gene associated with Lateral Meningocele Syndrome is NOTCH3 (Notch Receptor 3), and among its related pathways/superpathways are Gene expression (Transcription) and Infectious disease. Affiliated tissues include spinal cord and heart, and related phenotypes are ptosis and micrognathia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Newborn
<1/1000000
15
151
11

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

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PMID
Journal
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IF
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