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Echinobase
Summary Literature (0)
DOID:0070006 - Seckel syndrome 6

Disease Ontology Definition:A Seckel syndrome that has_material_basis_in homozygous mutation in the CEP63 gene on chromosome 3q22.

Synonyms: SCKL6,

Echinobase Genes : cep63


OMIM:
MIM:614728 - seckel syndrome 6; sckl6

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)