Term Name:	primary autosomal recessive microcephaly 7
Synonyms:	MCPH7
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the STIL gene on chromosome 1p33.
Ontology:	Human Disease [DOID:0070278]   ( DOID:0070278 )