Seckel syndrome 1

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Summary

Literature (0)

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: microcephalic primordial dwarfism I, SCKL1

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

: atr

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008869 - Seckel syndrome 1

MONDO:0008869 - Seckel syndrome 1

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)