lateral meningocele syndrome (DOID:0111343)
Alliance: disease page
Synonyms: Lehman syndrome
Alt IDs: OMIM:130720, MESH:C537878, ORDO:2789, UMLS_CUI:C1851710
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.