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Echinobase
Summary Literature (0)
DOID:0070012 - Seckel syndrome 5

Disease Ontology Definition:A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21.

Synonyms: SCKL5,

Echinobase Genes : cep152


OMIM:
MIM:613823 - seckel syndrome 5; sckl5

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)