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Echinobase
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 : dna2


OMIM:
MIM:615807 - seckel syndrome 8; sckl8

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Seckel syndrome (is_a)