Term Name: | primary autosomal recessive microcephaly 6 |
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Synonyms: | MCPH6 |
Definition: | A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CENPJ gene on chromosome 13q12. |
Ontology: | Human Disease [DOID:0070290] ( DOID:0070290 ) |