Term Name:	neurodevelopmental disorder with behavioral abnormalities and childhood-onset spastic paraplegia
Synonyms:	NEDBSPG
Definition:	A hereditary spastic paraplegia characterized by mild global developmental delay apparent from infancy, with mildly delayed walking and speech acquisition, mildly impaired intellectual development, behavioral abnormalities, and age-dependent, slowly progressive spastic paraplegia late in the first decade, resulting in gait abnormalities but not loss of ambulation, that has_material_basis_in homozygous mutation in the TBCB gene on chromosome 19q13.
Ontology:	Human Disease [DOID:0070718]   ( DOID:0070718 )