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Summary Literature (0)
DOID:0070009 - Seckel syndrome 8


Disease Ontology Definition:A Seckel syndrome that has_material_basis_in homozygous mutation in the DNA2 gene on chromosome 10q21.

Synonyms: SCKL8

Referenced OMIM:
OMIM:615807 - SECKEL SYNDROME 8; SCKL8

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : dna2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): Seckel syndrome (is_a)


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Version: 4.14.0
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