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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,
Xenbase Genes : cep63
MONDO:0013871 - Seckel syndrome 6 |
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)