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| Term | primary autosomal recessive microcephaly 25 | ID (Ontology) | DOID:0051036 (Human Disease) |
| Definition | A primary autosomal recessive microcephaly that has_material_basis_in homozygous mutation in the MAP11 gene on chromosome 7q22. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal recessive disease__ primary microcephaly_________| primary autosomal recessive microcephaly |__primary autosomal recessive microcephaly 25 |
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| Is a | primary autosomal recessive microcephaly | ||
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External Crossreferences & Linkouts
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| MIM:618351 | |||