Search Ontology:
Human Disease
Seckel syndrome 5
- Term ID
- DOID:0070012
- Synonyms
-
- SCKL5
- Definition
- A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/21131973
- References
- Ontology
- Human Disease ( DOID:0070012 )
- is a type of
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