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| Term | Seckel syndrome 8 | ID (Ontology) | DOID:0070009 (Human Disease) | |||||||||
| Definition | A Seckel syndrome that has_material_basis_in homozygous mutation in the DNA2 gene on chromosome 10q21. | |||||||||||
| Also Known As | "SCKL8" | |||||||||||
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| DO.org | ||||||||||||
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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__ syndrome_____________________| Seckel syndrome |__Seckel syndrome 8 1 rec. |
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| Is a | Seckel syndrome | ||
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| MIM:615807 | |||