Seckel syndrome 6

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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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cep63

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013871 - Seckel syndrome 6

MONDO:0013871 - Seckel syndrome 6

MIM:

MIM:614728 - SECKEL SYNDROME 6; SCKL6

MIM:614728 - SECKEL SYNDROME 6; SCKL6

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)