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Summary Literature (0)
MIM:613823 - SECKEL SYNDROME 5; SCKL5

Xenbase Genes: cep152

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013443 - Seckel syndrome 5
MONDO:0019342 - Seckel syndrome

Disease Ontology (DO):
DOID:0070012 - Seckel syndrome 5