Term Name: | primary autosomal recessive microcephaly 4 |
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Synonyms: | MCPH4 |
Definition: | A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the KNL1 gene on chromosome 15q15. |
Ontology: | Human Disease [DOID:0070291] ( DOID:0070291 ) |