lateral meningocele syndrome

Summary
Synonym
  • Lehman syndrome
Definition
A syndrome characterized by facial anomalies, hyperextensibility, hypotonia, and meningocele-related neurologic dysfunction that has_material_basis_in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.12.
Super Class
autosomal dominant disease syndrome
Disease Ontology
DOID:0111343
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4854 NOTCH3 notch receptor 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
18131 Notch3 notch 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
56761 Notch3 notch receptor 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
31293 N Notch
Displaying 1 entry
Gene ID Gene Symbol Description Source
176286 glp-1 glp-1/Notch intracellular domain

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024