Seckel syndrome

Summary

DOID:0050569 - Seckel syndrome

Disease Ontology Definition:A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability.

Synonyms: Harper's syndrome, Virchow-Seckel dwarfism, bird-headed dwarfism, microcephalic primordial dwarfism,

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

: plk4, atrip, traip, cenpe, cep63, nin, cep152, atr, cenpj, dna2, rbbp8, nsmce2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0019342 - Seckel syndrome

MONDO:0019342 - Seckel syndrome

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), syndrome (is_a)