Search Ontology:
Human Disease
Seckel syndrome 8
- Term ID
- DOID:0070009
- Synonyms
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- SCKL8
- Definition
- A Seckel syndrome that has_material_basis_in homozygous mutation in the DNA2 gene on chromosome 10q21. https://www.ncbi.nlm.nih.gov/pubmed/24389050
- References
- Ontology
- Human Disease ( DOID:0070009 )
- is a type of
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