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Metadata
ID	DOID:0070012
Name	Seckel syndrome 5
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
Xrefs	OMIM:613823
Synonyms	SCKL5 [EXACT]
Parent Relationships	is_a Seckel syndrome