Term Name:	primary autosomal recessive microcephaly 22
Synonyms:
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the NCAPD3 gene on chromosome 11q25.
Ontology:	Human Disease [DOID:0051033]   ( DOID:0051033 )