Term Name:	primary autosomal recessive microcephaly 10
Synonyms:	MCPH10
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the ZNF335 gene on chromosome 20q13.
Ontology:	Human Disease [DOID:0070294]   (DOID:0070294)