Search Ontology:
Human Disease
Seckel syndrome 7
- Term ID
- DOID:0070011
- Synonyms
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- SCKL7
- Definition
- A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NIN gene on chromosome 14q22. https://www.ncbi.nlm.nih.gov/pubmed/22933543
- References
- Ontology
- Human Disease ( DOID:0070011 )
- is a type of
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