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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

Xenbase Genes : cep152

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013443 - Seckel syndrome 5


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)