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 )

Relationships
is a type of: primary autosomal recessive microcephaly