| Term Name: | primary autosomal recessive microcephaly 23 |
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| Synonyms: | |
| Definition: | A primary autosomal recessive microcephaly that has_material_basis_in homozygous mutation in the NCAPH gene on chromosome 2q11. |
| Ontology: | Human Disease [DOID:0051034] ( DOID:0051034 ) |