Seckel syndrome 8

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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

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: dna2

MIM:

MIM:615807 - seckel syndrome 8; sckl8

MIM:615807 - seckel syndrome 8; sckl8

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): Seckel syndrome (is_a)