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Summary Literature (0)
DOID:0070011 - Seckel syndrome 7

Disease Ontology Definition:A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NIN gene on chromosome 14q22.

Synonyms: SCKL7,

Xenbase Genes : nin

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013922 - Seckel syndrome 7


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Seckel syndrome (is_a)