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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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models