Seckel syndrome 10

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Summary

Literature (0)

DOID:0070008 - Seckel syndrome 10

Disease Ontology Definition:A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NSMCE2 gene on chromosome 8q24.

Synonyms: SCKL10

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

: nsmce2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014991 - Seckel syndrome 10

MONDO:0014991 - Seckel syndrome 10

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)