Search Ontology:
Human Disease
Seckel syndrome 10
- Term ID
- DOID:0070008
- Synonyms
-
- SCKL10
- Definition
- A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NSMCE2 gene on chromosome 8q24. https://www.ncbi.nlm.nih.gov/pubmed/25105364
- References
- Ontology
- Human Disease ( DOID:0070008 )
- is a type of
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