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| General Information | |||
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| Term | autosomal dominant microcephaly | ID (Ontology) | DOID:14725 (Human Disease) |
| Definition | A microcephaly that has_material_basis_in heterozygous mutation in an autosomal gene. | ||
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| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease_________ congenital nervous system abnormality | |__microcephaly_______________________| autosomal dominant microcephaly |
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| Parents/Children View Depth |
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Relationships
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| Is a |
autosomal dominant disease microcephaly |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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MESH:C537323 MIM:156580 UMLS_CUI:C0220693 |
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