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Summary Literature (1)
DOID:0070007 - Seckel syndrome 1

Disease Ontology Definition:A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ATR gene on chromosome 3q23.

Synonyms: SCKL1, microcephalic primordial dwarfism I,

Xenbase Genes : atr

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008869 - Seckel syndrome 1


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)