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)

Relationships
is a type of: primary autosomal recessive microcephaly