Term Name:	primary autosomal recessive microcephaly 15
Synonyms:	MCPH15, NEDMISBA, neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities
Definition:	A primary autosomal recessive microcephaly characterized by impaired intellectual development with poor speech, progressive microcephaly, and appendicular spasticity that has_material_basis_in homozygous or compound heterozygous mutation in the MFSD2A gene on chromosome 1p34.
Ontology:	Human Disease [DOID:0070277]   ( DOID:0070277 )