Disease #04331 (LMNS (meningocele, lateral syndrome (LMNS)), OMIM:130720)

Official abbreviation LMNS
Name meningocele, lateral syndrome (LMNS)
OMIM ID 130720
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NOTCH3
Associated tissues -
Disease features -
Remarks -

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