Seckel syndrome 9

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Summary

Literature (0)

DOID:0070005 - Seckel syndrome 9

Disease Ontology Definition:A Seckel syndrome that has_material_basis_in homozygous mutation in the TRAIP gene on chromosome 3p21.

Synonyms: SCKL9

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

: traip

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014767 - left crus of diaphragm

MONDO:0014767 - left crus of diaphragm

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)