Term Name:	primary autosomal recessive microcephaly 11
Synonyms:	MCPH11
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the PHC1 gene on chromosome 12p13.
Ontology:	Human Disease [DOID:0070287]   ( DOID:0070287 )