Human genes for lateral meningocele syndrome
Lateral meningocele syndrome [DOID:0111343]
A syndrome characterized by facial anomalies, hyperextensibility, hypotonia, and meningocele-related neurologic dysfunction that has_material_basis_in heterozygous mutation in NOTCH3 on chromosome 19p13.12.
Synonyms: lateral meningocele syndrome, DOID:0111343, lateral meningocele disease, lateral meningocele disorder, lateral meningocele syndromes ...